Canonical Allele Identifier: CA347803397
Gene: ZAP70 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.97737547A>T , CM000664.2:g.97737547A>T GRCh38
NC_000002.11:g.98354010A>T , CM000664.1:g.98354010A>T GRCh37
NC_000002.10:g.97720442A>T NCBI36
NG_007727.1:g.28980A>T , LRG_126:g.28980A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000698508.1:c.1364A>T ENSP00000513759.1:p.Lys455Met
ENST00000698509.1:n.1504A>T
ENST00000264972.10:c.1364A>T MANE Select ENSP00000264972.5:p.Lys455Met
ENST00000264972.9:c.1364A>T ENSP00000264972.5:p.Lys455Met
ENST00000451498.2:c.443A>T ENSP00000400475.2:p.Lys148Met
ENST00000463643.5:n.1225A>T
ENST00000487283.5:n.2416A>T
ENST00000495754.1:n.302A>T
NM_001079.3:c.1364A>T , LRG_126t1:c.1364A>T NP_001070.2:p.Lys455Met
NM_207519.1:c.443A>T NP_997402.1:p.Lys148Met
XM_005264015.3:c.1346A>T XP_005264072.1:p.Lys449Met
XM_006712728.2:c.1364A>T XP_006712791.1:p.Lys455Met
XM_011511783.1:c.1364A>T XP_011510085.1:p.Lys455Met
XR_923018.1:n.1566A>T
XR_923019.1:n.1566A>T
XR_923020.1:n.1566A>T
XM_017004867.1:c.1733A>T XP_016860356.1:p.Lys578Met
XM_017004868.1:c.1715A>T XP_016860357.1:p.Lys572Met
XM_017004869.1:c.1733A>T XP_016860358.1:p.Lys578Met
XM_017004870.1:c.1733A>T XP_016860359.1:p.Lys578Met
XR_001738925.1:n.2972A>T
XR_001738926.1:n.2972A>T
XR_001738927.1:n.2972A>T
NM_001079.4:c.1364A>T MANE Select NP_001070.2:p.Lys455Met
NM_001378594.1:c.1364A>T NP_001365523.1:p.Lys455Met
NM_207519.2:c.443A>T NP_997402.1:p.Lys148Met