Canonical Allele Identifier: CA1273123218

Gene: ZAP70

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.97739388C= , CM000664.2:g.97739388C=	GRCh38
NC_000002.11:g.98355851C= , CM000664.1:g.98355851C=	GRCh37
NC_000002.10:g.97722283C=	NCBI36
NG_007727.1:g.30821C= , LRG_126:g.30821C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698508.1:c.1750C=	ENSP00000513759.1:p.Pro584=
ENST00000698509.1:n.1890C=
ENST00000264972.10:c.1750C= MANE Select	ENSP00000264972.5:p.Pro584=
ENST00000264972.9:c.1750C=	ENSP00000264972.5:p.Pro584=
ENST00000451498.2:c.829C=	ENSP00000400475.2:p.Pro277=
ENST00000463643.5:n.1611C=
ENST00000487283.5:n.2802C=
NM_001079.3:c.1750C= , LRG_126t1:c.1750C=	NP_001070.2:p.Pro584=
NM_207519.1:c.829C=	NP_997402.1:p.Pro277=
XM_005264015.3:c.1732C=	XP_005264072.1:p.Pro578=
XM_011511783.1:c.1736+1281C=	XP_011510085.1:n.1736+1281C=
XR_923018.1:n.1938+1281C=
XR_923019.1:n.1938+1281C=
XR_923020.1:n.2161C=
XM_017004867.1:c.2119C=	XP_016860356.1:p.Pro707=
XM_017004868.1:c.2101C=	XP_016860357.1:p.Pro701=
XM_017004869.1:c.2105+1281C=	XP_016860358.1:n.2105+1281C=
XR_001738925.1:n.3344+1281C=
XR_001738926.1:n.3344+1281C=
XR_001738927.1:n.3567C=
NM_001079.4:c.1750C= MANE Select	NP_001070.2:p.Pro584=
NM_001378594.1:c.1750C=	NP_001365523.1:p.Pro584=
NM_207519.2:c.829C=	NP_997402.1:p.Pro277=