Canonical Allele Identifier: CA347803506
Gene: ZAP70 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.97737577G>T , CM000664.2:g.97737577G>T GRCh38
NC_000002.11:g.98354040G>T , CM000664.1:g.98354040G>T GRCh37
NC_000002.10:g.97720472G>T NCBI36
NG_007727.1:g.29010G>T , LRG_126:g.29010G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000698508.1:c.1394G>T ENSP00000513759.1:p.Arg465Leu
ENST00000698509.1:n.1534G>T
ENST00000264972.10:c.1394G>T MANE Select ENSP00000264972.5:p.Arg465Leu
ENST00000264972.9:c.1394G>T ENSP00000264972.5:p.Arg465Leu
ENST00000451498.2:c.473G>T ENSP00000400475.2:p.Arg158Leu
ENST00000463643.5:n.1255G>T
ENST00000487283.5:n.2446G>T
ENST00000495754.1:n.332G>T
NM_001079.3:c.1394G>T , LRG_126t1:c.1394G>T NP_001070.2:p.Arg465Leu
NM_207519.1:c.473G>T NP_997402.1:p.Arg158Leu
XM_005264015.3:c.1376G>T XP_005264072.1:p.Arg459Leu
XM_006712728.2:c.1394G>T XP_006712791.1:p.Arg465Leu
XM_011511783.1:c.1394G>T XP_011510085.1:p.Arg465Leu
XR_923018.1:n.1596G>T
XR_923019.1:n.1596G>T
XR_923020.1:n.1596G>T
XM_017004867.1:c.1763G>T XP_016860356.1:p.Arg588Leu
XM_017004868.1:c.1745G>T XP_016860357.1:p.Arg582Leu
XM_017004869.1:c.1763G>T XP_016860358.1:p.Arg588Leu
XM_017004870.1:c.1763G>T XP_016860359.1:p.Arg588Leu
XR_001738925.1:n.3002G>T
XR_001738926.1:n.3002G>T
XR_001738927.1:n.3002G>T
NM_001079.4:c.1394G>T MANE Select NP_001070.2:p.Arg465Leu
NM_001378594.1:c.1394G>T NP_001365523.1:p.Arg465Leu
NM_207519.2:c.473G>T NP_997402.1:p.Arg158Leu