Canonical Allele Identifier: CA347803244

Gene: ZAP70

Linked Data

• MyVariant Identifiers: chr2:g.98353949G>C (hg19) ; chr2:g.97737486G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.97737486G>C , CM000664.2:g.97737486G>C	GRCh38
NC_000002.11:g.98353949G>C , CM000664.1:g.98353949G>C	GRCh37
NC_000002.10:g.97720381G>C	NCBI36
NG_007727.1:g.28919G>C , LRG_126:g.28919G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000698508.1:c.1303G>C	ENSP00000513759.1:p.Val435Leu
ENST00000698509.1:n.1443G>C
ENST00000264972.10:c.1303G>C MANE Select	ENSP00000264972.5:p.Val435Leu
ENST00000264972.9:c.1303G>C	ENSP00000264972.5:p.Val435Leu
ENST00000451498.2:c.382G>C	ENSP00000400475.2:p.Val128Leu
ENST00000463643.5:n.1164G>C
ENST00000487283.5:n.2355G>C
ENST00000495754.1:n.241G>C
NM_001079.3:c.1303G>C , LRG_126t1:c.1303G>C	NP_001070.2:p.Val435Leu
NM_207519.1:c.382G>C	NP_997402.1:p.Val128Leu
XM_005264015.3:c.1285G>C	XP_005264072.1:p.Val429Leu
XM_006712728.2:c.1303G>C	XP_006712791.1:p.Val435Leu
XM_011511783.1:c.1303G>C	XP_011510085.1:p.Val435Leu
XR_923018.1:n.1505G>C
XR_923019.1:n.1505G>C
XR_923020.1:n.1505G>C
XM_017004867.1:c.1672G>C	XP_016860356.1:p.Val558Leu
XM_017004868.1:c.1654G>C	XP_016860357.1:p.Val552Leu
XM_017004869.1:c.1672G>C	XP_016860358.1:p.Val558Leu
XM_017004870.1:c.1672G>C	XP_016860359.1:p.Val558Leu
XR_001738925.1:n.2911G>C
XR_001738926.1:n.2911G>C
XR_001738927.1:n.2911G>C
NM_001079.4:c.1303G>C MANE Select	NP_001070.2:p.Val435Leu
NM_001378594.1:c.1303G>C	NP_001365523.1:p.Val435Leu
NM_207519.2:c.382G>C	NP_997402.1:p.Val128Leu