Canonical Allele Identifier: CA343936
Gene: ZAP70 HGNC NCBI

Linked Data

ClinVar Variation Id: 41039
ClinVar RCV Id: RCV000033937
dbSNP Id: rs113994173

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.97733464G>A , CM000664.2:g.97733464G>A GRCh38
NC_000002.11:g.98349927G>A , CM000664.1:g.98349927G>A GRCh37
NC_000002.10:g.97716359G>A NCBI36
NG_007727.1:g.24897G>A , LRG_126:g.24897G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000698508.1:c.838-80G>A ENSP00000513759.1:n.838-80G>A
ENST00000698509.1:n.978-80G>A
ENST00000264972.10:c.838-80G>A MANE Select ENSP00000264972.5:n.838-80G>A
ENST00000264972.9:c.838-80G>A ENSP00000264972.5:n.838-80G>A
ENST00000463643.5:n.699-80G>A
ENST00000483781.5:n.1151G>A
ENST00000487283.5:n.349G>A
NM_001079.3:c.838-80G>A , LRG_126t1:c.838-80G>A NP_001070.2:n.838-80G>A
XM_005264015.3:c.838-80G>A XP_005264072.1:n.838-80G>A
XM_006712728.2:c.838-80G>A XP_006712791.1:n.838-80G>A
XM_011511783.1:c.838-80G>A XP_011510085.1:n.838-80G>A
XR_923018.1:n.1040-80G>A
XR_923019.1:n.1040-80G>A
XR_923020.1:n.1040-80G>A
XM_017004867.1:c.1207-80G>A XP_016860356.1:n.1207-80G>A
XM_017004868.1:c.1207-80G>A XP_016860357.1:n.1207-80G>A
XM_017004869.1:c.1207-80G>A XP_016860358.1:n.1207-80G>A
XM_017004870.1:c.1207-80G>A XP_016860359.1:n.1207-80G>A
XR_001738925.1:n.2446-80G>A
XR_001738926.1:n.2446-80G>A
XR_001738927.1:n.2446-80G>A
NM_001079.4:c.838-80G>A MANE Select NP_001070.2:n.838-80G>A
NM_001378594.1:c.838-80G>A NP_001365523.1:n.838-80G>A
NM_207519.2:c.-1088G>A NP_997402.1:n.-1088G>A