Canonical Allele Identifier: CA1273123216

Gene: ZAP70

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.97739385C= , CM000664.2:g.97739385C=	GRCh38
NC_000002.11:g.98355848C= , CM000664.1:g.98355848C=	GRCh37
NC_000002.10:g.97722280C=	NCBI36
NG_007727.1:g.30818C= , LRG_126:g.30818C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698508.1:c.1747C=	ENSP00000513759.1:p.Arg583=
ENST00000698509.1:n.1887C=
ENST00000264972.10:c.1747C= MANE Select	ENSP00000264972.5:p.Arg583=
ENST00000264972.9:c.1747C=	ENSP00000264972.5:p.Arg583=
ENST00000451498.2:c.826C=	ENSP00000400475.2:p.Arg276=
ENST00000463643.5:n.1608C=
ENST00000487283.5:n.2799C=
NM_001079.3:c.1747C= , LRG_126t1:c.1747C=	NP_001070.2:p.Arg583=
NM_207519.1:c.826C=	NP_997402.1:p.Arg276=
XM_005264015.3:c.1729C=	XP_005264072.1:p.Arg577=
XM_011511783.1:c.1736+1278C=	XP_011510085.1:n.1736+1278C=
XR_923018.1:n.1938+1278C=
XR_923019.1:n.1938+1278C=
XR_923020.1:n.2158C=
XM_017004867.1:c.2116C=	XP_016860356.1:p.Arg706=
XM_017004868.1:c.2098C=	XP_016860357.1:p.Arg700=
XM_017004869.1:c.2105+1278C=	XP_016860358.1:n.2105+1278C=
XR_001738925.1:n.3344+1278C=
XR_001738926.1:n.3344+1278C=
XR_001738927.1:n.3564C=
NM_001079.4:c.1747C= MANE Select	NP_001070.2:p.Arg583=
NM_001378594.1:c.1747C=	NP_001365523.1:p.Arg583=
NM_207519.2:c.826C=	NP_997402.1:p.Arg276=