Canonical Allele Identifier: CA347803246
Gene: ZAP70 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.97737487T>A , CM000664.2:g.97737487T>A GRCh38
NC_000002.11:g.98353950T>A , CM000664.1:g.98353950T>A GRCh37
NC_000002.10:g.97720382T>A NCBI36
NG_007727.1:g.28920T>A , LRG_126:g.28920T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000698508.1:c.1304T>A ENSP00000513759.1:p.Val435Glu
ENST00000698509.1:n.1444T>A
ENST00000264972.10:c.1304T>A MANE Select ENSP00000264972.5:p.Val435Glu
ENST00000264972.9:c.1304T>A ENSP00000264972.5:p.Val435Glu
ENST00000451498.2:c.383T>A ENSP00000400475.2:p.Val128Glu
ENST00000463643.5:n.1165T>A
ENST00000487283.5:n.2356T>A
ENST00000495754.1:n.242T>A
NM_001079.3:c.1304T>A , LRG_126t1:c.1304T>A NP_001070.2:p.Val435Glu
NM_207519.1:c.383T>A NP_997402.1:p.Val128Glu
XM_005264015.3:c.1286T>A XP_005264072.1:p.Val429Glu
XM_006712728.2:c.1304T>A XP_006712791.1:p.Val435Glu
XM_011511783.1:c.1304T>A XP_011510085.1:p.Val435Glu
XR_923018.1:n.1506T>A
XR_923019.1:n.1506T>A
XR_923020.1:n.1506T>A
XM_017004867.1:c.1673T>A XP_016860356.1:p.Val558Glu
XM_017004868.1:c.1655T>A XP_016860357.1:p.Val552Glu
XM_017004869.1:c.1673T>A XP_016860358.1:p.Val558Glu
XM_017004870.1:c.1673T>A XP_016860359.1:p.Val558Glu
XR_001738925.1:n.2912T>A
XR_001738926.1:n.2912T>A
XR_001738927.1:n.2912T>A
NM_001079.4:c.1304T>A MANE Select NP_001070.2:p.Val435Glu
NM_001378594.1:c.1304T>A NP_001365523.1:p.Val435Glu
NM_207519.2:c.383T>A NP_997402.1:p.Val128Glu