Canonical Allele Identifier: CA347803220
Gene: ZAP70 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.97737476G>C , CM000664.2:g.97737476G>C GRCh38
NC_000002.11:g.98353939G>C , CM000664.1:g.98353939G>C GRCh37
NC_000002.10:g.97720371G>C NCBI36
NG_007727.1:g.28909G>C , LRG_126:g.28909G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000698508.1:c.1293G>C ENSP00000513759.1:p.Glu431Asp
ENST00000698509.1:n.1433G>C
ENST00000264972.10:c.1293G>C MANE Select ENSP00000264972.5:p.Glu431Asp
ENST00000264972.9:c.1293G>C ENSP00000264972.5:p.Glu431Asp
ENST00000451498.2:c.372G>C ENSP00000400475.2:p.Glu124Asp
ENST00000463643.5:n.1154G>C
ENST00000487283.5:n.2345G>C
ENST00000495754.1:n.231G>C
NM_001079.3:c.1293G>C , LRG_126t1:c.1293G>C NP_001070.2:p.Glu431Asp
NM_207519.1:c.372G>C NP_997402.1:p.Glu124Asp
XM_005264015.3:c.1275G>C XP_005264072.1:p.Glu425Asp
XM_006712728.2:c.1293G>C XP_006712791.1:p.Glu431Asp
XM_011511783.1:c.1293G>C XP_011510085.1:p.Glu431Asp
XR_923018.1:n.1495G>C
XR_923019.1:n.1495G>C
XR_923020.1:n.1495G>C
XM_017004867.1:c.1662G>C XP_016860356.1:p.Glu554Asp
XM_017004868.1:c.1644G>C XP_016860357.1:p.Glu548Asp
XM_017004869.1:c.1662G>C XP_016860358.1:p.Glu554Asp
XM_017004870.1:c.1662G>C XP_016860359.1:p.Glu554Asp
XR_001738925.1:n.2901G>C
XR_001738926.1:n.2901G>C
XR_001738927.1:n.2901G>C
NM_001079.4:c.1293G>C MANE Select NP_001070.2:p.Glu431Asp
NM_001378594.1:c.1293G>C NP_001365523.1:p.Glu431Asp
NM_207519.2:c.372G>C NP_997402.1:p.Glu124Asp