Canonical Allele Identifier: CA360484861

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.96762274A>T , CM000667.2:g.96762274A>T GRCh38
NC_000005.9:g.96097978A>T , CM000667.1:g.96097978A>T GRCh37
NC_000005.8:g.96123734A>T NCBI36
NG_027839.1:g.56871T>A
NG_029490.1:g.105238A>T
NG_027839.2:g.178710T>A
NG_029490.2:g.105238A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000484552.6:c.754A>T (CAST) ENSP00000432878.2:p.Lys252Ter
ENST00000508608.6:c.1684A>T (CAST) ENSP00000422677.2:p.Lys562Ter
ENST00000510756.6:c.1462A>T (CAST) ENSP00000422176.2:p.Lys488Ter
ENST00000674587.1:c.1291A>T (CAST) ENSP00000501797.1:p.Lys431Ter
ENST00000674702.1:c.1576A>T (CAST) ENSP00000502345.1:p.Lys526Ter
ENST00000674984.1:c.1768A>T (CAST) ENSP00000501713.1:p.Lys590Ter
ENST00000675033.1:c.1462A>T (CAST) ENSP00000501659.1:p.Lys488Ter
ENST00000675179.1:c.1834A>T (CAST) MANE Select ENSP00000501872.1:p.Lys612Ter
ENST00000675185.1:c.215A>T (CAST)
ENST00000675266.1:c.1736A>T (CAST)
ENST00000675267.1:c.*1458A>T (CAST) ENSP00000502095.1:n.*1458A>T
ENST00000675275.1:c.551A>T (CAST)
ENST00000675479.1:c.1447A>T (CAST) ENSP00000502244.1:p.Lys483Ter
ENST00000675614.1:c.1504A>T (CAST) ENSP00000502136.1:p.Lys502Ter
ENST00000675663.1:c.1723A>T (CAST) ENSP00000502449.1:p.Lys575Ter
ENST00000675734.1:n.378A>T (CAST)
ENST00000675858.1:c.1378A>T (CAST) ENSP00000501780.1:p.Lys460Ter
ENST00000296754.7:c.*926T>A (ERAP1) ENSP00000296754.3:n.*926T>A
ENST00000309190.9:c.1519A>T (CAST) ENSP00000312523.5:p.Lys507Ter
ENST00000325674.11:c.754A>T (CAST) ENSP00000320319.8:p.Lys252Ter
ENST00000338252.7:c.1546A>T (CAST) ENSP00000343421.3:p.Lys516Ter
ENST00000341926.7:c.1585A>T (CAST) ENSP00000339914.3:p.Lys529Ter
ENST00000348386.7:n.1527A>T (CAST)
ENST00000395812.6:c.1711A>T (CAST) ENSP00000379157.2:p.Lys571Ter
ENST00000395813.5:c.1585A>T (CAST) ENSP00000379158.2:p.Lys529Ter
ENST00000437034.6:c.840A>T (CAST)
ENST00000484552.5:c.812A>T (CAST)
ENST00000504465.5:c.1369A>T (CAST) ENSP00000425670.1:p.Lys457Ter
ENST00000508579.5:c.730A>T (CAST) ENSP00000425787.1:p.Lys244Ter
ENST00000508608.5:c.1723A>T (CAST) ENSP00000422677.1:p.Lys575Ter
ENST00000508830.5:c.1834A>T (CAST) ENSP00000425721.1:p.Lys612Ter
ENST00000509903.5:c.1480A>T (CAST) ENSP00000426946.1:p.Lys494Ter
ENST00000510098.1:c.70A>T (CAST) ENSP00000427195.1:p.Lys24Ter
ENST00000510156.5:c.1585A>T (CAST) ENSP00000422325.1:p.Lys529Ter
ENST00000510500.5:c.857A>T (CAST)
ENST00000510756.5:c.1768A>T (CAST) ENSP00000422176.1:p.Lys590Ter
ENST00000511049.5:c.1543A>T (CAST) ENSP00000421130.1:p.Lys515Ter
ENST00000511782.5:c.1543A>T (CAST) ENSP00000423638.1:p.Lys515Ter
ENST00000515663.5:c.754A>T (CAST) ENSP00000422929.1:p.Lys252Ter
NM_001042440.3:c.1711A>T (CAST) NP_001035905.1:p.Lys571Ter
NM_001190442.1:c.1546A>T (CAST) NP_001177371.1:p.Lys516Ter
NM_001284212.1:c.1462A>T (CAST) NP_001271141.1:p.Lys488Ter
NM_001284213.1:c.1369A>T (CAST) NP_001271142.1:p.Lys457Ter
NM_016442.3:c.*926T>A (ERAP1) NP_057526.3:n.*926T>A
NM_173060.3:c.1519A>T (CAST) NP_775083.1:p.Lys507Ter
NR_104285.1:n.841A>T (CAST)
XM_006714696.2:c.1834A>T (CAST) XP_006714759.1:p.Lys612Ter
XM_006714697.2:c.1834A>T (CAST) XP_006714760.1:p.Lys612Ter
XM_006714698.2:c.1795A>T (CAST) XP_006714761.1:p.Lys599Ter
XM_006714699.2:c.1789A>T (CAST) XP_006714762.1:p.Lys597Ter
XM_006714700.2:c.1777A>T (CAST) XP_006714763.1:p.Lys593Ter
XM_006714701.2:c.1768A>T (CAST) XP_006714764.1:p.Lys590Ter
XM_006714702.2:c.1732A>T (CAST) XP_006714765.1:p.Lys578Ter
XM_006714703.2:c.1729A>T (CAST) XP_006714766.1:p.Lys577Ter
XM_006714704.2:c.1723A>T (CAST) XP_006714767.1:p.Lys575Ter
XM_006714705.2:c.1711A>T (CAST) XP_006714768.1:p.Lys571Ter
XM_006714706.2:c.1666A>T (CAST) XP_006714769.1:p.Lys556Ter
XM_006714707.2:c.1585A>T (CAST) XP_006714770.1:p.Lys529Ter
XM_006714708.2:c.1546A>T (CAST) XP_006714771.1:p.Lys516Ter
XM_006714709.2:c.1528A>T (CAST) XP_006714772.1:p.Lys510Ter
XM_006714710.2:c.1480A>T (CAST) XP_006714773.1:p.Lys494Ter
XM_006714711.2:c.1462A>T (CAST) XP_006714774.1:p.Lys488Ter
XM_006714712.2:c.1423A>T (CAST) XP_006714775.1:p.Lys475Ter
XM_006714713.2:c.754A>T (CAST) XP_006714776.1:p.Lys252Ter
XM_006714714.2:c.754A>T (CAST) XP_006714777.1:p.Lys252Ter
XM_006714715.2:c.730A>T (CAST) XP_006714778.1:p.Lys244Ter
XM_011543487.1:c.*926T>A (ERAP1) XP_011541789.1:n.*926T>A
XM_011543654.1:c.1753A>T (CAST) XP_011541956.1:p.Lys585Ter
XM_011543655.1:c.1750A>T (CAST) XP_011541957.1:p.Lys584Ter
XM_011543656.1:c.1687A>T (CAST) XP_011541958.1:p.Lys563Ter
XM_011543657.1:c.1642A>T (CAST) XP_011541959.1:p.Lys548Ter
XM_011543658.1:c.1438A>T (CAST) XP_011541960.1:p.Lys480Ter
NM_001042440.4:c.1711A>T (CAST) NP_001035905.1:p.Lys571Ter
NM_001042441.2:c.1777A>T (CAST) NP_001035906.1:p.Lys593Ter
NM_001042442.2:c.1768A>T (CAST) NP_001035907.1:p.Lys590Ter
NM_001042443.2:c.1585A>T (CAST) NP_001035908.1:p.Lys529Ter
NM_001042444.2:c.1462A>T (CAST) NP_001035909.1:p.Lys488Ter
NM_001042445.2:c.1480A>T (CAST) NP_001035910.1:p.Lys494Ter
NM_001042446.2:c.1423A>T (CAST) NP_001035911.1:p.Lys475Ter
NM_001284212.3:c.1462A>T (CAST) NP_001271141.1:p.Lys488Ter
NM_001284213.3:c.1369A>T (CAST) NP_001271142.1:p.Lys457Ter
NM_001330626.1:c.1738A>T (CAST) NP_001317555.1:p.Lys580Ter
NM_001330627.1:c.1711A>T (CAST) NP_001317556.1:p.Lys571Ter
NM_001330628.1:c.1666A>T (CAST) NP_001317557.1:p.Lys556Ter
NM_001330629.1:c.1750A>T (CAST) NP_001317558.1:p.Lys584Ter
NM_001330630.1:c.1423A>T (CAST) NP_001317559.1:p.Lys475Ter
NM_001330631.1:c.1546A>T (CAST) NP_001317560.1:p.Lys516Ter
NM_001330632.1:c.1519A>T (CAST) NP_001317561.1:p.Lys507Ter
NM_001330633.1:c.1528A>T (CAST) NP_001317562.1:p.Lys510Ter
NM_001330634.1:c.1489A>T (CAST) NP_001317563.1:p.Lys497Ter
NM_001349244.1:c.*926T>A (ERAP1) NP_001336173.1:n.*926T>A
NM_001750.6:c.1834A>T (CAST) NP_001741.4:p.Lys612Ter
NM_016442.4:c.*926T>A (ERAP1) NP_057526.3:n.*926T>A
NM_173060.4:c.1519A>T (CAST) NP_775083.1:p.Lys507Ter
XR_001742119.2:n.3911T>A (ERAP1)
NM_001042440.5:c.1711A>T (CAST) NP_001035905.1:p.Lys571Ter
NM_001042441.3:c.1777A>T (CAST) NP_001035906.1:p.Lys593Ter
NM_001042442.3:c.1768A>T (CAST) NP_001035907.1:p.Lys590Ter
NM_001330626.2:c.1738A>T (CAST) NP_001317555.1:p.Lys580Ter
NM_001330627.2:c.1711A>T (CAST) NP_001317556.1:p.Lys571Ter
NM_001330628.2:c.1666A>T (CAST) NP_001317557.1:p.Lys556Ter
NM_001330629.2:c.1750A>T (CAST) NP_001317558.1:p.Lys584Ter
NM_001375317.1:c.1723A>T (CAST) NP_001362246.1:p.Lys575Ter
NM_001750.7:c.1834A>T (CAST) MANE Select NP_001741.4:p.Lys612Ter
NR_104285.2:n.779A>T (CAST)
NM_001042443.3:c.1585A>T (CAST) NP_001035908.1:p.Lys529Ter
NM_001042444.3:c.1462A>T (CAST) NP_001035909.1:p.Lys488Ter
NM_001042445.3:c.1480A>T (CAST) NP_001035910.1:p.Lys494Ter
NM_001042446.3:c.1423A>T (CAST) NP_001035911.1:p.Lys475Ter
NM_001190442.2:c.1546A>T (CAST) NP_001177371.1:p.Lys516Ter
NM_001284212.4:c.1462A>T (CAST) NP_001271141.1:p.Lys488Ter
NM_001284213.4:c.1369A>T (CAST) NP_001271142.1:p.Lys457Ter
NM_001330630.2:c.1423A>T (CAST) NP_001317559.1:p.Lys475Ter
NM_001330631.2:c.1546A>T (CAST) NP_001317560.1:p.Lys516Ter
NM_001330632.2:c.1519A>T (CAST) NP_001317561.1:p.Lys507Ter
NM_001330633.2:c.1528A>T (CAST) NP_001317562.1:p.Lys510Ter
NM_001330634.2:c.1489A>T (CAST) NP_001317563.1:p.Lys497Ter
NM_001349244.2:c.*926T>A (ERAP1) NP_001336173.1:n.*926T>A
NM_016442.5:c.*926T>A (ERAP1) NP_057526.3:n.*926T>A
NM_173060.5:c.1519A>T (CAST) NP_775083.1:p.Lys507Ter