Canonical Allele Identifier: CA360484906

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.96762295G>C , CM000667.2:g.96762295G>C GRCh38
NC_000005.9:g.96097999G>C , CM000667.1:g.96097999G>C GRCh37
NC_000005.8:g.96123755G>C NCBI36
NG_027839.1:g.56850C>G
NG_029490.1:g.105259G>C
NG_027839.2:g.178689C>G
NG_029490.2:g.105259G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000484552.6:c.775G>C (CAST) ENSP00000432878.2:p.Ala259Pro
ENST00000508608.6:c.1705G>C (CAST) ENSP00000422677.2:p.Ala569Pro
ENST00000510756.6:c.1483G>C (CAST) ENSP00000422176.2:p.Ala495Pro
ENST00000674587.1:c.1312G>C (CAST) ENSP00000501797.1:p.Ala438Pro
ENST00000674702.1:c.1597G>C (CAST) ENSP00000502345.1:p.Ala533Pro
ENST00000674984.1:c.1789G>C (CAST) ENSP00000501713.1:p.Ala597Pro
ENST00000675033.1:c.1483G>C (CAST) ENSP00000501659.1:p.Ala495Pro
ENST00000675179.1:c.1855G>C (CAST) MANE Select ENSP00000501872.1:p.Ala619Pro
ENST00000675185.1:c.236G>C (CAST)
ENST00000675266.1:c.1757G>C (CAST)
ENST00000675267.1:c.*1479G>C (CAST) ENSP00000502095.1:n.*1479G>C
ENST00000675275.1:c.572G>C (CAST)
ENST00000675479.1:c.1468G>C (CAST) ENSP00000502244.1:p.Ala490Pro
ENST00000675614.1:c.1525G>C (CAST) ENSP00000502136.1:p.Ala509Pro
ENST00000675663.1:c.1744G>C (CAST) ENSP00000502449.1:p.Ala582Pro
ENST00000675734.1:n.399G>C (CAST)
ENST00000675858.1:c.1399G>C (CAST) ENSP00000501780.1:p.Ala467Pro
ENST00000296754.7:c.*905C>G (ERAP1) ENSP00000296754.3:n.*905C>G
ENST00000309190.9:c.1540G>C (CAST) ENSP00000312523.5:p.Ala514Pro
ENST00000325674.11:c.775G>C (CAST) ENSP00000320319.8:p.Ala259Pro
ENST00000338252.7:c.1567G>C (CAST) ENSP00000343421.3:p.Ala523Pro
ENST00000341926.7:c.1606G>C (CAST) ENSP00000339914.3:p.Ala536Pro
ENST00000348386.7:n.1548G>C (CAST)
ENST00000395812.6:c.1732G>C (CAST) ENSP00000379157.2:p.Ala578Pro
ENST00000395813.5:c.1606G>C (CAST) ENSP00000379158.2:p.Ala536Pro
ENST00000437034.6:c.861G>C (CAST)
ENST00000484552.5:c.833G>C (CAST)
ENST00000504465.5:c.1390G>C (CAST) ENSP00000425670.1:p.Ala464Pro
ENST00000508579.5:c.751G>C (CAST) ENSP00000425787.1:p.Ala251Pro
ENST00000508608.5:c.1744G>C (CAST) ENSP00000422677.1:p.Ala582Pro
ENST00000508830.5:c.1855G>C (CAST) ENSP00000425721.1:p.Ala619Pro
ENST00000509903.5:c.1501G>C (CAST) ENSP00000426946.1:p.Ala501Pro
ENST00000510098.1:c.91G>C (CAST) ENSP00000427195.1:p.Ala31Pro
ENST00000510156.5:c.1606G>C (CAST) ENSP00000422325.1:p.Ala536Pro
ENST00000510500.5:c.878G>C (CAST)
ENST00000510756.5:c.1789G>C (CAST) ENSP00000422176.1:p.Ala597Pro
ENST00000511049.5:c.1564G>C (CAST) ENSP00000421130.1:p.Ala522Pro
ENST00000511782.5:c.1564G>C (CAST) ENSP00000423638.1:p.Ala522Pro
ENST00000515663.5:c.775G>C (CAST) ENSP00000422929.1:p.Ala259Pro
NM_001042440.3:c.1732G>C (CAST) NP_001035905.1:p.Ala578Pro
NM_001190442.1:c.1567G>C (CAST) NP_001177371.1:p.Ala523Pro
NM_001284212.1:c.1483G>C (CAST) NP_001271141.1:p.Ala495Pro
NM_001284213.1:c.1390G>C (CAST) NP_001271142.1:p.Ala464Pro
NM_016442.3:c.*905C>G (ERAP1) NP_057526.3:n.*905C>G
NM_173060.3:c.1540G>C (CAST) NP_775083.1:p.Ala514Pro
NR_104285.1:n.862G>C (CAST)
XM_006714696.2:c.1855G>C (CAST) XP_006714759.1:p.Ala619Pro
XM_006714697.2:c.1855G>C (CAST) XP_006714760.1:p.Ala619Pro
XM_006714698.2:c.1816G>C (CAST) XP_006714761.1:p.Ala606Pro
XM_006714699.2:c.1810G>C (CAST) XP_006714762.1:p.Ala604Pro
XM_006714700.2:c.1798G>C (CAST) XP_006714763.1:p.Ala600Pro
XM_006714701.2:c.1789G>C (CAST) XP_006714764.1:p.Ala597Pro
XM_006714702.2:c.1753G>C (CAST) XP_006714765.1:p.Ala585Pro
XM_006714703.2:c.1750G>C (CAST) XP_006714766.1:p.Ala584Pro
XM_006714704.2:c.1744G>C (CAST) XP_006714767.1:p.Ala582Pro
XM_006714705.2:c.1732G>C (CAST) XP_006714768.1:p.Ala578Pro
XM_006714706.2:c.1687G>C (CAST) XP_006714769.1:p.Ala563Pro
XM_006714707.2:c.1606G>C (CAST) XP_006714770.1:p.Ala536Pro
XM_006714708.2:c.1567G>C (CAST) XP_006714771.1:p.Ala523Pro
XM_006714709.2:c.1549G>C (CAST) XP_006714772.1:p.Ala517Pro
XM_006714710.2:c.1501G>C (CAST) XP_006714773.1:p.Ala501Pro
XM_006714711.2:c.1483G>C (CAST) XP_006714774.1:p.Ala495Pro
XM_006714712.2:c.1444G>C (CAST) XP_006714775.1:p.Ala482Pro
XM_006714713.2:c.775G>C (CAST) XP_006714776.1:p.Ala259Pro
XM_006714714.2:c.775G>C (CAST) XP_006714777.1:p.Ala259Pro
XM_006714715.2:c.751G>C (CAST) XP_006714778.1:p.Ala251Pro
XM_011543487.1:c.*905C>G (ERAP1) XP_011541789.1:n.*905C>G
XM_011543654.1:c.1774G>C (CAST) XP_011541956.1:p.Ala592Pro
XM_011543655.1:c.1771G>C (CAST) XP_011541957.1:p.Ala591Pro
XM_011543656.1:c.1708G>C (CAST) XP_011541958.1:p.Ala570Pro
XM_011543657.1:c.1663G>C (CAST) XP_011541959.1:p.Ala555Pro
XM_011543658.1:c.1459G>C (CAST) XP_011541960.1:p.Ala487Pro
NM_001042440.4:c.1732G>C (CAST) NP_001035905.1:p.Ala578Pro
NM_001042441.2:c.1798G>C (CAST) NP_001035906.1:p.Ala600Pro
NM_001042442.2:c.1789G>C (CAST) NP_001035907.1:p.Ala597Pro
NM_001042443.2:c.1606G>C (CAST) NP_001035908.1:p.Ala536Pro
NM_001042444.2:c.1483G>C (CAST) NP_001035909.1:p.Ala495Pro
NM_001042445.2:c.1501G>C (CAST) NP_001035910.1:p.Ala501Pro
NM_001042446.2:c.1444G>C (CAST) NP_001035911.1:p.Ala482Pro
NM_001284212.3:c.1483G>C (CAST) NP_001271141.1:p.Ala495Pro
NM_001284213.3:c.1390G>C (CAST) NP_001271142.1:p.Ala464Pro
NM_001330626.1:c.1759G>C (CAST) NP_001317555.1:p.Ala587Pro
NM_001330627.1:c.1732G>C (CAST) NP_001317556.1:p.Ala578Pro
NM_001330628.1:c.1687G>C (CAST) NP_001317557.1:p.Ala563Pro
NM_001330629.1:c.1771G>C (CAST) NP_001317558.1:p.Ala591Pro
NM_001330630.1:c.1444G>C (CAST) NP_001317559.1:p.Ala482Pro
NM_001330631.1:c.1567G>C (CAST) NP_001317560.1:p.Ala523Pro
NM_001330632.1:c.1540G>C (CAST) NP_001317561.1:p.Ala514Pro
NM_001330633.1:c.1549G>C (CAST) NP_001317562.1:p.Ala517Pro
NM_001330634.1:c.1510G>C (CAST) NP_001317563.1:p.Ala504Pro
NM_001349244.1:c.*905C>G (ERAP1) NP_001336173.1:n.*905C>G
NM_001750.6:c.1855G>C (CAST) NP_001741.4:p.Ala619Pro
NM_016442.4:c.*905C>G (ERAP1) NP_057526.3:n.*905C>G
NM_173060.4:c.1540G>C (CAST) NP_775083.1:p.Ala514Pro
XR_001742119.2:n.3890C>G (ERAP1)
NM_001042440.5:c.1732G>C (CAST) NP_001035905.1:p.Ala578Pro
NM_001042441.3:c.1798G>C (CAST) NP_001035906.1:p.Ala600Pro
NM_001042442.3:c.1789G>C (CAST) NP_001035907.1:p.Ala597Pro
NM_001330626.2:c.1759G>C (CAST) NP_001317555.1:p.Ala587Pro
NM_001330627.2:c.1732G>C (CAST) NP_001317556.1:p.Ala578Pro
NM_001330628.2:c.1687G>C (CAST) NP_001317557.1:p.Ala563Pro
NM_001330629.2:c.1771G>C (CAST) NP_001317558.1:p.Ala591Pro
NM_001375317.1:c.1744G>C (CAST) NP_001362246.1:p.Ala582Pro
NM_001750.7:c.1855G>C (CAST) MANE Select NP_001741.4:p.Ala619Pro
NR_104285.2:n.800G>C (CAST)
NM_001042443.3:c.1606G>C (CAST) NP_001035908.1:p.Ala536Pro
NM_001042444.3:c.1483G>C (CAST) NP_001035909.1:p.Ala495Pro
NM_001042445.3:c.1501G>C (CAST) NP_001035910.1:p.Ala501Pro
NM_001042446.3:c.1444G>C (CAST) NP_001035911.1:p.Ala482Pro
NM_001190442.2:c.1567G>C (CAST) NP_001177371.1:p.Ala523Pro
NM_001284212.4:c.1483G>C (CAST) NP_001271141.1:p.Ala495Pro
NM_001284213.4:c.1390G>C (CAST) NP_001271142.1:p.Ala464Pro
NM_001330630.2:c.1444G>C (CAST) NP_001317559.1:p.Ala482Pro
NM_001330631.2:c.1567G>C (CAST) NP_001317560.1:p.Ala523Pro
NM_001330632.2:c.1540G>C (CAST) NP_001317561.1:p.Ala514Pro
NM_001330633.2:c.1549G>C (CAST) NP_001317562.1:p.Ala517Pro
NM_001330634.2:c.1510G>C (CAST) NP_001317563.1:p.Ala504Pro
NM_001349244.2:c.*905C>G (ERAP1) NP_001336173.1:n.*905C>G
NM_016442.5:c.*905C>G (ERAP1) NP_057526.3:n.*905C>G
NM_173060.5:c.1540G>C (CAST) NP_775083.1:p.Ala514Pro