Canonical Allele Identifier: CA1273123176

Gene: ZAP70

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.97739297A= , CM000664.2:g.97739297A=	GRCh38
NC_000002.11:g.98355760A= , CM000664.1:g.98355760A=	GRCh37
NC_000002.10:g.97722192A=	NCBI36
NG_007727.1:g.30730A= , LRG_126:g.30730A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000698508.1:c.1737-78A=	ENSP00000513759.1:n.1737-78A=
ENST00000698509.1:n.1877-78A=
ENST00000264972.10:c.1737-78A= MANE Select	ENSP00000264972.5:n.1737-78A=
ENST00000264972.9:c.1737-78A=	ENSP00000264972.5:n.1737-78A=
ENST00000451498.2:c.816-78A=	ENSP00000400475.2:n.816-78A=
ENST00000463643.5:n.1598-78A=
ENST00000487283.5:n.2789-78A=
NM_001079.3:c.1737-78A= , LRG_126t1:c.1737-78A=	NP_001070.2:n.1737-78A=
NM_207519.1:c.816-78A=	NP_997402.1:n.816-78A=
XM_005264015.3:c.1719-78A=	XP_005264072.1:n.1719-78A=
XM_011511783.1:c.1736+1190A=	XP_011510085.1:n.1736+1190A=
XR_923018.1:n.1938+1190A=
XR_923019.1:n.1938+1190A=
XR_923020.1:n.2148-78A=
XM_017004867.1:c.2106-78A=	XP_016860356.1:n.2106-78A=
XM_017004868.1:c.2088-78A=	XP_016860357.1:n.2088-78A=
XM_017004869.1:c.2105+1190A=	XP_016860358.1:n.2105+1190A=
XR_001738925.1:n.3344+1190A=
XR_001738926.1:n.3344+1190A=
XR_001738927.1:n.3554-78A=
NM_001079.4:c.1737-78A= MANE Select	NP_001070.2:n.1737-78A=
NM_001378594.1:c.1737-78A=	NP_001365523.1:n.1737-78A=
NM_207519.2:c.816-78A=	NP_997402.1:n.816-78A=