Canonical Allele Identifier: CA1790598

Gene: ZAP70

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.97739527G>A , CM000664.2:g.97739527G>A	GRCh38
NC_000002.11:g.98355990G>A , CM000664.1:g.98355990G>A	GRCh37
NC_000002.10:g.97722422G>A	NCBI36
NG_007727.1:g.30960G>A , LRG_126:g.30960G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698508.1:c.*29G>A	ENSP00000513759.1:n.*29G>A
ENST00000698509.1:n.2029G>A
ENST00000264972.10:c.*29G>A MANE Select	ENSP00000264972.5:n.*29G>A
ENST00000264972.9:c.*29G>A	ENSP00000264972.5:n.*29G>A
ENST00000463643.5:n.1750G>A
ENST00000487283.5:n.2941G>A
NM_001079.3:c.*29G>A , LRG_126t1:c.*29G>A	NP_001070.2:n.*29G>A
NM_207519.1:c.*29G>A	NP_997402.1:n.*29G>A
XM_005264015.3:c.*29G>A	XP_005264072.1:n.*29G>A
XM_011511783.1:c.1736+1420G>A	XP_011510085.1:n.1736+1420G>A
XR_923018.1:n.1938+1420G>A
XR_923019.1:n.1938+1420G>A
XM_017004867.1:c.*29G>A	XP_016860356.1:n.*29G>A
XM_017004868.1:c.*29G>A	XP_016860357.1:n.*29G>A
XM_017004869.1:c.2105+1420G>A	XP_016860358.1:n.2105+1420G>A
XR_001738925.1:n.3344+1420G>A
XR_001738926.1:n.3344+1420G>A
NM_001079.4:c.*29G>A MANE Select	NP_001070.2:n.*29G>A
NM_001378594.1:c.*29G>A	NP_001365523.1:n.*29G>A
NM_207519.2:c.*29G>A	NP_997402.1:n.*29G>A