Canonical Allele Identifier: CA1273122323
Gene: ZAP70 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.97737490G= , CM000664.2:g.97737490G= GRCh38
NC_000002.11:g.98353953G= , CM000664.1:g.98353953G= GRCh37
NC_000002.10:g.97720385G= NCBI36
NG_007727.1:g.28923G= , LRG_126:g.28923G=

Transcript Alleles

HGVS Amino-acid change
ENST00000698508.1:c.1307G= ENSP00000513759.1:p.Ser436=
ENST00000698509.1:n.1447G=
ENST00000264972.10:c.1307G= MANE Select ENSP00000264972.5:p.Ser436=
ENST00000264972.9:c.1307G= ENSP00000264972.5:p.Ser436=
ENST00000451498.2:c.386G= ENSP00000400475.2:p.Ser129=
ENST00000463643.5:n.1168G=
ENST00000487283.5:n.2359G=
ENST00000495754.1:n.245G=
NM_001079.3:c.1307G= , LRG_126t1:c.1307G= NP_001070.2:p.Ser436=
NM_207519.1:c.386G= NP_997402.1:p.Ser129=
XM_005264015.3:c.1289G= XP_005264072.1:p.Ser430=
XM_006712728.2:c.1307G= XP_006712791.1:p.Ser436=
XM_011511783.1:c.1307G= XP_011510085.1:p.Ser436=
XR_923018.1:n.1509G=
XR_923019.1:n.1509G=
XR_923020.1:n.1509G=
XM_017004867.1:c.1676G= XP_016860356.1:p.Ser559=
XM_017004868.1:c.1658G= XP_016860357.1:p.Ser553=
XM_017004869.1:c.1676G= XP_016860358.1:p.Ser559=
XM_017004870.1:c.1676G= XP_016860359.1:p.Ser559=
XR_001738925.1:n.2915G=
XR_001738926.1:n.2915G=
XR_001738927.1:n.2915G=
NM_001079.4:c.1307G= MANE Select NP_001070.2:p.Ser436=
NM_001378594.1:c.1307G= NP_001365523.1:p.Ser436=
NM_207519.2:c.386G= NP_997402.1:p.Ser129=