Canonical Allele Identifier: CA1273122350
Gene: ZAP70 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.97737576C= , CM000664.2:g.97737576C= GRCh38
NC_000002.11:g.98354039C= , CM000664.1:g.98354039C= GRCh37
NC_000002.10:g.97720471C= NCBI36
NG_007727.1:g.29009C= , LRG_126:g.29009C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000698508.1:c.1393C= ENSP00000513759.1:p.Arg465=
ENST00000698509.1:n.1533C=
ENST00000264972.10:c.1393C= MANE Select ENSP00000264972.5:p.Arg465=
ENST00000264972.9:c.1393C= ENSP00000264972.5:p.Arg465=
ENST00000451498.2:c.472C= ENSP00000400475.2:p.Arg158=
ENST00000463643.5:n.1254C=
ENST00000487283.5:n.2445C=
ENST00000495754.1:n.331C=
NM_001079.3:c.1393C= , LRG_126t1:c.1393C= NP_001070.2:p.Arg465=
NM_207519.1:c.472C= NP_997402.1:p.Arg158=
XM_005264015.3:c.1375C= XP_005264072.1:p.Arg459=
XM_006712728.2:c.1393C= XP_006712791.1:p.Arg465=
XM_011511783.1:c.1393C= XP_011510085.1:p.Arg465=
XR_923018.1:n.1595C=
XR_923019.1:n.1595C=
XR_923020.1:n.1595C=
XM_017004867.1:c.1762C= XP_016860356.1:p.Arg588=
XM_017004868.1:c.1744C= XP_016860357.1:p.Arg582=
XM_017004869.1:c.1762C= XP_016860358.1:p.Arg588=
XM_017004870.1:c.1762C= XP_016860359.1:p.Arg588=
XR_001738925.1:n.3001C=
XR_001738926.1:n.3001C=
XR_001738927.1:n.3001C=
NM_001079.4:c.1393C= MANE Select NP_001070.2:p.Arg465=
NM_001378594.1:c.1393C= NP_001365523.1:p.Arg465=
NM_207519.2:c.472C= NP_997402.1:p.Arg158=