Canonical Allele Identifier: CA1565569286

Gene: CAST ERAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.96762318T= , CM000667.2:g.96762318T=	GRCh38
NC_000005.9:g.96098022T= , CM000667.1:g.96098022T=	GRCh37
NC_000005.8:g.96123778T=	NCBI36
NG_027839.1:g.56827A=
NG_029490.1:g.105282T=
NG_027839.2:g.178666A=
NG_029490.2:g.105282T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000484552.6:c.798T= (CAST)	ENSP00000432878.2:p.Val266=
ENST00000508608.6:c.1728T= (CAST)	ENSP00000422677.2:p.Val576=
ENST00000510756.6:c.1506T= (CAST)	ENSP00000422176.2:p.Val502=
ENST00000674587.1:c.1335T= (CAST)	ENSP00000501797.1:p.Val445=
ENST00000674702.1:c.1620T= (CAST)	ENSP00000502345.1:p.Val540=
ENST00000674984.1:c.1812T= (CAST)	ENSP00000501713.1:p.Val604=
ENST00000675033.1:c.1506T= (CAST)	ENSP00000501659.1:p.Val502=
ENST00000675179.1:c.1878T= (CAST) MANE Select	ENSP00000501872.1:p.Val626=
ENST00000675185.1:c.259T= (CAST)
ENST00000675266.1:c.1780T= (CAST)
ENST00000675267.1:c.*1502T= (CAST)	ENSP00000502095.1:n.*1502T=
ENST00000675275.1:c.595T= (CAST)
ENST00000675479.1:c.1491T= (CAST)	ENSP00000502244.1:p.Val497=
ENST00000675614.1:c.1548T= (CAST)	ENSP00000502136.1:p.Val516=
ENST00000675663.1:c.1767T= (CAST)	ENSP00000502449.1:p.Val589=
ENST00000675734.1:n.422T= (CAST)
ENST00000675858.1:c.1422T= (CAST)	ENSP00000501780.1:p.Val474=
ENST00000296754.7:c.*882A= (ERAP1)	ENSP00000296754.3:n.*882A=
ENST00000309190.9:c.1563T= (CAST)	ENSP00000312523.5:p.Val521=
ENST00000325674.11:c.798T= (CAST)	ENSP00000320319.8:p.Val266=
ENST00000338252.7:c.1590T= (CAST)	ENSP00000343421.3:p.Val530=
ENST00000341926.7:c.1629T= (CAST)	ENSP00000339914.3:p.Val543=
ENST00000348386.7:n.1571T= (CAST)
ENST00000395812.6:c.1755T= (CAST)	ENSP00000379157.2:p.Val585=
ENST00000395813.5:c.1629T= (CAST)	ENSP00000379158.2:p.Val543=
ENST00000437034.6:c.884T= (CAST)
ENST00000484552.5:c.856T= (CAST)
ENST00000504465.5:c.1413T= (CAST)	ENSP00000425670.1:p.Val471=
ENST00000508579.5:c.774T= (CAST)	ENSP00000425787.1:p.Val258=
ENST00000508608.5:c.1767T= (CAST)	ENSP00000422677.1:p.Val589=
ENST00000508830.5:c.1878T= (CAST)	ENSP00000425721.1:p.Val626=
ENST00000509903.5:c.1524T= (CAST)	ENSP00000426946.1:p.Val508=
ENST00000510098.1:c.114T= (CAST)	ENSP00000427195.1:p.Val38=
ENST00000510156.5:c.1629T= (CAST)	ENSP00000422325.1:p.Val543=
ENST00000510500.5:c.901T= (CAST)
ENST00000510756.5:c.1812T= (CAST)	ENSP00000422176.1:p.Val604=
ENST00000511049.5:c.1587T= (CAST)	ENSP00000421130.1:p.Val529=
ENST00000511782.5:c.1587T= (CAST)	ENSP00000423638.1:p.Val529=
ENST00000515663.5:c.798T= (CAST)	ENSP00000422929.1:p.Val266=
NM_001042440.3:c.1755T= (CAST)	NP_001035905.1:p.Val585=
NM_001190442.1:c.1590T= (CAST)	NP_001177371.1:p.Val530=
NM_001284212.1:c.1506T= (CAST)	NP_001271141.1:p.Val502=
NM_001284213.1:c.1413T= (CAST)	NP_001271142.1:p.Val471=
NM_016442.3:c.*882A= (ERAP1)	NP_057526.3:n.*882A=
NM_173060.3:c.1563T= (CAST)	NP_775083.1:p.Val521=
NR_104285.1:n.885T= (CAST)
XM_006714696.2:c.1878T= (CAST)	XP_006714759.1:p.Val626=
XM_006714697.2:c.1878T= (CAST)	XP_006714760.1:p.Val626=
XM_006714698.2:c.1839T= (CAST)	XP_006714761.1:p.Val613=
XM_006714699.2:c.1833T= (CAST)	XP_006714762.1:p.Val611=
XM_006714700.2:c.1821T= (CAST)	XP_006714763.1:p.Val607=
XM_006714701.2:c.1812T= (CAST)	XP_006714764.1:p.Val604=
XM_006714702.2:c.1776T= (CAST)	XP_006714765.1:p.Val592=
XM_006714703.2:c.1773T= (CAST)	XP_006714766.1:p.Val591=
XM_006714704.2:c.1767T= (CAST)	XP_006714767.1:p.Val589=
XM_006714705.2:c.1755T= (CAST)	XP_006714768.1:p.Val585=
XM_006714706.2:c.1710T= (CAST)	XP_006714769.1:p.Val570=
XM_006714707.2:c.1629T= (CAST)	XP_006714770.1:p.Val543=
XM_006714708.2:c.1590T= (CAST)	XP_006714771.1:p.Val530=
XM_006714709.2:c.1572T= (CAST)	XP_006714772.1:p.Val524=
XM_006714710.2:c.1524T= (CAST)	XP_006714773.1:p.Val508=
XM_006714711.2:c.1506T= (CAST)	XP_006714774.1:p.Val502=
XM_006714712.2:c.1467T= (CAST)	XP_006714775.1:p.Val489=
XM_006714713.2:c.798T= (CAST)	XP_006714776.1:p.Val266=
XM_006714714.2:c.798T= (CAST)	XP_006714777.1:p.Val266=
XM_006714715.2:c.774T= (CAST)	XP_006714778.1:p.Val258=
XM_011543487.1:c.*882A= (ERAP1)	XP_011541789.1:n.*882A=
XM_011543654.1:c.1797T= (CAST)	XP_011541956.1:p.Val599=
XM_011543655.1:c.1794T= (CAST)	XP_011541957.1:p.Val598=
XM_011543656.1:c.1731T= (CAST)	XP_011541958.1:p.Val577=
XM_011543657.1:c.1686T= (CAST)	XP_011541959.1:p.Val562=
XM_011543658.1:c.1482T= (CAST)	XP_011541960.1:p.Val494=
NM_001042440.4:c.1755T= (CAST)	NP_001035905.1:p.Val585=
NM_001042441.2:c.1821T= (CAST)	NP_001035906.1:p.Val607=
NM_001042442.2:c.1812T= (CAST)	NP_001035907.1:p.Val604=
NM_001042443.2:c.1629T= (CAST)	NP_001035908.1:p.Val543=
NM_001042444.2:c.1506T= (CAST)	NP_001035909.1:p.Val502=
NM_001042445.2:c.1524T= (CAST)	NP_001035910.1:p.Val508=
NM_001042446.2:c.1467T= (CAST)	NP_001035911.1:p.Val489=
NM_001284212.3:c.1506T= (CAST)	NP_001271141.1:p.Val502=
NM_001284213.3:c.1413T= (CAST)	NP_001271142.1:p.Val471=
NM_001330626.1:c.1782T= (CAST)	NP_001317555.1:p.Val594=
NM_001330627.1:c.1755T= (CAST)	NP_001317556.1:p.Val585=
NM_001330628.1:c.1710T= (CAST)	NP_001317557.1:p.Val570=
NM_001330629.1:c.1794T= (CAST)	NP_001317558.1:p.Val598=
NM_001330630.1:c.1467T= (CAST)	NP_001317559.1:p.Val489=
NM_001330631.1:c.1590T= (CAST)	NP_001317560.1:p.Val530=
NM_001330632.1:c.1563T= (CAST)	NP_001317561.1:p.Val521=
NM_001330633.1:c.1572T= (CAST)	NP_001317562.1:p.Val524=
NM_001330634.1:c.1533T= (CAST)	NP_001317563.1:p.Val511=
NM_001349244.1:c.*882A= (ERAP1)	NP_001336173.1:n.*882A=
NM_001750.6:c.1878T= (CAST)	NP_001741.4:p.Val626=
NM_016442.4:c.*882A= (ERAP1)	NP_057526.3:n.*882A=
NM_173060.4:c.1563T= (CAST)	NP_775083.1:p.Val521=
XR_001742119.2:n.3867A= (ERAP1)
NM_001042440.5:c.1755T= (CAST)	NP_001035905.1:p.Val585=
NM_001042441.3:c.1821T= (CAST)	NP_001035906.1:p.Val607=
NM_001042442.3:c.1812T= (CAST)	NP_001035907.1:p.Val604=
NM_001330626.2:c.1782T= (CAST)	NP_001317555.1:p.Val594=
NM_001330627.2:c.1755T= (CAST)	NP_001317556.1:p.Val585=
NM_001330628.2:c.1710T= (CAST)	NP_001317557.1:p.Val570=
NM_001330629.2:c.1794T= (CAST)	NP_001317558.1:p.Val598=
NM_001375317.1:c.1767T= (CAST)	NP_001362246.1:p.Val589=
NM_001750.7:c.1878T= (CAST) MANE Select	NP_001741.4:p.Val626=
NR_104285.2:n.823T= (CAST)
NM_001042443.3:c.1629T= (CAST)	NP_001035908.1:p.Val543=
NM_001042444.3:c.1506T= (CAST)	NP_001035909.1:p.Val502=
NM_001042445.3:c.1524T= (CAST)	NP_001035910.1:p.Val508=
NM_001042446.3:c.1467T= (CAST)	NP_001035911.1:p.Val489=
NM_001190442.2:c.1590T= (CAST)	NP_001177371.1:p.Val530=
NM_001284212.4:c.1506T= (CAST)	NP_001271141.1:p.Val502=
NM_001284213.4:c.1413T= (CAST)	NP_001271142.1:p.Val471=
NM_001330630.2:c.1467T= (CAST)	NP_001317559.1:p.Val489=
NM_001330631.2:c.1590T= (CAST)	NP_001317560.1:p.Val530=
NM_001330632.2:c.1563T= (CAST)	NP_001317561.1:p.Val521=
NM_001330633.2:c.1572T= (CAST)	NP_001317562.1:p.Val524=
NM_001330634.2:c.1533T= (CAST)	NP_001317563.1:p.Val511=
NM_001349244.2:c.*882A= (ERAP1)	NP_001336173.1:n.*882A=
NM_016442.5:c.*882A= (ERAP1)	NP_057526.3:n.*882A=
NM_173060.5:c.1563T= (CAST)	NP_775083.1:p.Val521=