Canonical Allele Identifier: CA343164
Gene: ZAP70 HGNC NCBI

Linked Data

ClinVar Variation Id: 38913
ClinVar RCV Id: RCV000032161
dbSNP Id: rs113994175

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.97738085A>T , CM000664.2:g.97738085A>T GRCh38
NC_000002.11:g.98354548A>T , CM000664.1:g.98354548A>T GRCh37
NC_000002.10:g.97720980A>T NCBI36
NG_007727.1:g.29518A>T , LRG_126:g.29518A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000698508.1:c.1714A>T ENSP00000513759.1:p.Met572Leu
ENST00000698509.1:n.1854A>T
ENST00000264972.10:c.1714A>T MANE Select ENSP00000264972.5:p.Met572Leu
ENST00000264972.9:c.1714A>T ENSP00000264972.5:p.Met572Leu
ENST00000451498.2:c.793A>T ENSP00000400475.2:p.Met265Leu
ENST00000463643.5:n.1575A>T
ENST00000487283.5:n.2766A>T
ENST00000489250.1:n.167A>T
NM_001079.3:c.1714A>T , LRG_126t1:c.1714A>T NP_001070.2:p.Met572Leu
NM_207519.1:c.793A>T NP_997402.1:p.Met265Leu
XM_005264015.3:c.1696A>T XP_005264072.1:p.Met566Leu
XM_006712728.2:c.1714A>T XP_006712791.1:p.Met572Leu
XM_011511783.1:c.1714A>T XP_011510085.1:p.Met572Leu
XR_923018.1:n.1916A>T
XR_923019.1:n.1916A>T
XR_923020.1:n.1916A>T
XM_017004867.1:c.2083A>T XP_016860356.1:p.Met695Leu
XM_017004868.1:c.2065A>T XP_016860357.1:p.Met689Leu
XM_017004869.1:c.2083A>T XP_016860358.1:p.Met695Leu
XM_017004870.1:c.2083A>T XP_016860359.1:p.Met695Leu
XR_001738925.1:n.3322A>T
XR_001738926.1:n.3322A>T
XR_001738927.1:n.3322A>T
NM_001079.4:c.1714A>T MANE Select NP_001070.2:p.Met572Leu
NM_001378594.1:c.1714A>T NP_001365523.1:p.Met572Leu
NM_207519.2:c.793A>T NP_997402.1:p.Met265Leu