Canonical Allele Identifier: CA347803355
Gene: ZAP70 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.97737536C>A , CM000664.2:g.97737536C>A GRCh38
NC_000002.11:g.98353999C>A , CM000664.1:g.98353999C>A GRCh37
NC_000002.10:g.97720431C>A NCBI36
NG_007727.1:g.28969C>A , LRG_126:g.28969C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000698508.1:c.1353C>A ENSP00000513759.1:p.Tyr451Ter
ENST00000698509.1:n.1493C>A
ENST00000264972.10:c.1353C>A MANE Select ENSP00000264972.5:p.Tyr451Ter
ENST00000264972.9:c.1353C>A ENSP00000264972.5:p.Tyr451Ter
ENST00000451498.2:c.432C>A ENSP00000400475.2:p.Tyr144Ter
ENST00000463643.5:n.1214C>A
ENST00000487283.5:n.2405C>A
ENST00000495754.1:n.291C>A
NM_001079.3:c.1353C>A , LRG_126t1:c.1353C>A NP_001070.2:p.Tyr451Ter
NM_207519.1:c.432C>A NP_997402.1:p.Tyr144Ter
XM_005264015.3:c.1335C>A XP_005264072.1:p.Tyr445Ter
XM_006712728.2:c.1353C>A XP_006712791.1:p.Tyr451Ter
XM_011511783.1:c.1353C>A XP_011510085.1:p.Tyr451Ter
XR_923018.1:n.1555C>A
XR_923019.1:n.1555C>A
XR_923020.1:n.1555C>A
XM_017004867.1:c.1722C>A XP_016860356.1:p.Tyr574Ter
XM_017004868.1:c.1704C>A XP_016860357.1:p.Tyr568Ter
XM_017004869.1:c.1722C>A XP_016860358.1:p.Tyr574Ter
XM_017004870.1:c.1722C>A XP_016860359.1:p.Tyr574Ter
XR_001738925.1:n.2961C>A
XR_001738926.1:n.2961C>A
XR_001738927.1:n.2961C>A
NM_001079.4:c.1353C>A MANE Select NP_001070.2:p.Tyr451Ter
NM_001378594.1:c.1353C>A NP_001365523.1:p.Tyr451Ter
NM_207519.2:c.432C>A NP_997402.1:p.Tyr144Ter