Canonical Allele Identifier: CA347803472

Gene: ZAP70

Linked Data

• COSMIC: COSM2913655
• MyVariant Identifiers: chr2:g.98354030C>A (hg19) ; chr2:g.97737567C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.97737567C>A , CM000664.2:g.97737567C>A	GRCh38
NC_000002.11:g.98354030C>A , CM000664.1:g.98354030C>A	GRCh37
NC_000002.10:g.97720462C>A	NCBI36
NG_007727.1:g.29000C>A , LRG_126:g.29000C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698508.1:c.1384C>A	ENSP00000513759.1:p.Leu462Met
ENST00000698509.1:n.1524C>A
ENST00000264972.10:c.1384C>A MANE Select	ENSP00000264972.5:p.Leu462Met
ENST00000264972.9:c.1384C>A	ENSP00000264972.5:p.Leu462Met
ENST00000451498.2:c.463C>A	ENSP00000400475.2:p.Leu155Met
ENST00000463643.5:n.1245C>A
ENST00000487283.5:n.2436C>A
ENST00000495754.1:n.322C>A
NM_001079.3:c.1384C>A , LRG_126t1:c.1384C>A	NP_001070.2:p.Leu462Met
NM_207519.1:c.463C>A	NP_997402.1:p.Leu155Met
XM_005264015.3:c.1366C>A	XP_005264072.1:p.Leu456Met
XM_006712728.2:c.1384C>A	XP_006712791.1:p.Leu462Met
XM_011511783.1:c.1384C>A	XP_011510085.1:p.Leu462Met
XR_923018.1:n.1586C>A
XR_923019.1:n.1586C>A
XR_923020.1:n.1586C>A
XM_017004867.1:c.1753C>A	XP_016860356.1:p.Leu585Met
XM_017004868.1:c.1735C>A	XP_016860357.1:p.Leu579Met
XM_017004869.1:c.1753C>A	XP_016860358.1:p.Leu585Met
XM_017004870.1:c.1753C>A	XP_016860359.1:p.Leu585Met
XR_001738925.1:n.2992C>A
XR_001738926.1:n.2992C>A
XR_001738927.1:n.2992C>A
NM_001079.4:c.1384C>A MANE Select	NP_001070.2:p.Leu462Met
NM_001378594.1:c.1384C>A	NP_001365523.1:p.Leu462Met
NM_207519.2:c.463C>A	NP_997402.1:p.Leu155Met