Canonical Allele Identifier: CA347805055
Gene: ZAP70 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.97738001A>G , CM000664.2:g.97738001A>G GRCh38
NC_000002.11:g.98354464A>G , CM000664.1:g.98354464A>G GRCh37
NC_000002.10:g.97720896A>G NCBI36
NG_007727.1:g.29434A>G , LRG_126:g.29434A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000698508.1:c.1630A>G ENSP00000513759.1:p.Lys544Glu
ENST00000698509.1:n.1770A>G
ENST00000264972.10:c.1630A>G MANE Select ENSP00000264972.5:p.Lys544Glu
ENST00000264972.9:c.1630A>G ENSP00000264972.5:p.Lys544Glu
ENST00000451498.2:c.709A>G ENSP00000400475.2:p.Lys237Glu
ENST00000463643.5:n.1491A>G
ENST00000487283.5:n.2682A>G
ENST00000489250.1:n.83A>G
ENST00000495754.1:n.665A>G
NM_001079.3:c.1630A>G , LRG_126t1:c.1630A>G NP_001070.2:p.Lys544Glu
NM_207519.1:c.709A>G NP_997402.1:p.Lys237Glu
XM_005264015.3:c.1612A>G XP_005264072.1:p.Lys538Glu
XM_006712728.2:c.1630A>G XP_006712791.1:p.Lys544Glu
XM_011511783.1:c.1630A>G XP_011510085.1:p.Lys544Glu
XR_923018.1:n.1832A>G
XR_923019.1:n.1832A>G
XR_923020.1:n.1832A>G
XM_017004867.1:c.1999A>G XP_016860356.1:p.Lys667Glu
XM_017004868.1:c.1981A>G XP_016860357.1:p.Lys661Glu
XM_017004869.1:c.1999A>G XP_016860358.1:p.Lys667Glu
XM_017004870.1:c.1999A>G XP_016860359.1:p.Lys667Glu
XR_001738925.1:n.3238A>G
XR_001738926.1:n.3238A>G
XR_001738927.1:n.3238A>G
NM_001079.4:c.1630A>G MANE Select NP_001070.2:p.Lys544Glu
NM_001378594.1:c.1630A>G NP_001365523.1:p.Lys544Glu
NM_207519.2:c.709A>G NP_997402.1:p.Lys237Glu