Canonical Allele Identifier: CA1790440
Gene: ZAP70 HGNC NCBI

Linked Data

dbSNP Id: rs747461254
gnomAD v2: 2-98353953-G-A
gnomAD v3: 2-97737490-G-A
gnomAD v4: 2-97737490-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.97737490G>A , CM000664.2:g.97737490G>A GRCh38
NC_000002.11:g.98353953G>A , CM000664.1:g.98353953G>A GRCh37
NC_000002.10:g.97720385G>A NCBI36
NG_007727.1:g.28923G>A , LRG_126:g.28923G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000698508.1:c.1307G>A ENSP00000513759.1:p.Ser436Asn
ENST00000698509.1:n.1447G>A
ENST00000264972.10:c.1307G>A MANE Select ENSP00000264972.5:p.Ser436Asn
ENST00000264972.9:c.1307G>A ENSP00000264972.5:p.Ser436Asn
ENST00000451498.2:c.386G>A ENSP00000400475.2:p.Ser129Asn
ENST00000463643.5:n.1168G>A
ENST00000487283.5:n.2359G>A
ENST00000495754.1:n.245G>A
NM_001079.3:c.1307G>A , LRG_126t1:c.1307G>A NP_001070.2:p.Ser436Asn
NM_207519.1:c.386G>A NP_997402.1:p.Ser129Asn
XM_005264015.3:c.1289G>A XP_005264072.1:p.Ser430Asn
XM_006712728.2:c.1307G>A XP_006712791.1:p.Ser436Asn
XM_011511783.1:c.1307G>A XP_011510085.1:p.Ser436Asn
XR_923018.1:n.1509G>A
XR_923019.1:n.1509G>A
XR_923020.1:n.1509G>A
XM_017004867.1:c.1676G>A XP_016860356.1:p.Ser559Asn
XM_017004868.1:c.1658G>A XP_016860357.1:p.Ser553Asn
XM_017004869.1:c.1676G>A XP_016860358.1:p.Ser559Asn
XM_017004870.1:c.1676G>A XP_016860359.1:p.Ser559Asn
XR_001738925.1:n.2915G>A
XR_001738926.1:n.2915G>A
XR_001738927.1:n.2915G>A
NM_001079.4:c.1307G>A MANE Select NP_001070.2:p.Ser436Asn
NM_001378594.1:c.1307G>A NP_001365523.1:p.Ser436Asn
NM_207519.2:c.386G>A NP_997402.1:p.Ser129Asn