Canonical Allele Identifier: CA1790439

Gene: ZAP70

Linked Data

• ClinVar Variation Id: 1896174
• ClinVar RCV Id: RCV002575044
• dbSNP Id: rs778361599
• ExAC: 2:98353951 G / A
• gnomAD v2: 2-98353951-G-A
• gnomAD v4: 2-97737488-G-A
• MyVariant Identifiers: chr2:g.98353951G>A (hg19) ; chr2:g.97737488G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.97737488G>A , CM000664.2:g.97737488G>A	GRCh38
NC_000002.11:g.98353951G>A , CM000664.1:g.98353951G>A	GRCh37
NC_000002.10:g.97720383G>A	NCBI36
NG_007727.1:g.28921G>A , LRG_126:g.28921G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000698508.1:c.1305G>A	ENSP00000513759.1:p.Val435=
ENST00000698509.1:n.1445G>A
ENST00000264972.10:c.1305G>A MANE Select	ENSP00000264972.5:p.Val435=
ENST00000264972.9:c.1305G>A	ENSP00000264972.5:p.Val435=
ENST00000451498.2:c.384G>A	ENSP00000400475.2:p.Val128=
ENST00000463643.5:n.1166G>A
ENST00000487283.5:n.2357G>A
ENST00000495754.1:n.243G>A
NM_001079.3:c.1305G>A , LRG_126t1:c.1305G>A	NP_001070.2:p.Val435=
NM_207519.1:c.384G>A	NP_997402.1:p.Val128=
XM_005264015.3:c.1287G>A	XP_005264072.1:p.Val429=
XM_006712728.2:c.1305G>A	XP_006712791.1:p.Val435=
XM_011511783.1:c.1305G>A	XP_011510085.1:p.Val435=
XR_923018.1:n.1507G>A
XR_923019.1:n.1507G>A
XR_923020.1:n.1507G>A
XM_017004867.1:c.1674G>A	XP_016860356.1:p.Val558=
XM_017004868.1:c.1656G>A	XP_016860357.1:p.Val552=
XM_017004869.1:c.1674G>A	XP_016860358.1:p.Val558=
XM_017004870.1:c.1674G>A	XP_016860359.1:p.Val558=
XR_001738925.1:n.2913G>A
XR_001738926.1:n.2913G>A
XR_001738927.1:n.2913G>A
NM_001079.4:c.1305G>A MANE Select	NP_001070.2:p.Val435=
NM_001378594.1:c.1305G>A	NP_001365523.1:p.Val435=
NM_207519.2:c.384G>A	NP_997402.1:p.Val128=