Canonical Allele Identifier: CA347805002
Gene: ZAP70 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.97737995A>T , CM000664.2:g.97737995A>T GRCh38
NC_000002.11:g.98354458A>T , CM000664.1:g.98354458A>T GRCh37
NC_000002.10:g.97720890A>T NCBI36
NG_007727.1:g.29428A>T , LRG_126:g.29428A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000698508.1:c.1624A>T ENSP00000513759.1:p.Lys542Ter
ENST00000698509.1:n.1764A>T
ENST00000264972.10:c.1624A>T MANE Select ENSP00000264972.5:p.Lys542Ter
ENST00000264972.9:c.1624A>T ENSP00000264972.5:p.Lys542Ter
ENST00000451498.2:c.703A>T ENSP00000400475.2:p.Lys235Ter
ENST00000463643.5:n.1485A>T
ENST00000487283.5:n.2676A>T
ENST00000489250.1:n.77A>T
ENST00000495754.1:n.659A>T
NM_001079.3:c.1624A>T , LRG_126t1:c.1624A>T NP_001070.2:p.Lys542Ter
NM_207519.1:c.703A>T NP_997402.1:p.Lys235Ter
XM_005264015.3:c.1606A>T XP_005264072.1:p.Lys536Ter
XM_006712728.2:c.1624A>T XP_006712791.1:p.Lys542Ter
XM_011511783.1:c.1624A>T XP_011510085.1:p.Lys542Ter
XR_923018.1:n.1826A>T
XR_923019.1:n.1826A>T
XR_923020.1:n.1826A>T
XM_017004867.1:c.1993A>T XP_016860356.1:p.Lys665Ter
XM_017004868.1:c.1975A>T XP_016860357.1:p.Lys659Ter
XM_017004869.1:c.1993A>T XP_016860358.1:p.Lys665Ter
XM_017004870.1:c.1993A>T XP_016860359.1:p.Lys665Ter
XR_001738925.1:n.3232A>T
XR_001738926.1:n.3232A>T
XR_001738927.1:n.3232A>T
NM_001079.4:c.1624A>T MANE Select NP_001070.2:p.Lys542Ter
NM_001378594.1:c.1624A>T NP_001365523.1:p.Lys542Ter
NM_207519.2:c.703A>T NP_997402.1:p.Lys235Ter