Canonical Allele Identifier: CA173996
Gene: CTLA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 161112
ClinVar RCV Id: RCV000148293
dbSNP Id: rs606231420

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203868047C>A , CM000664.2:g.203868047C>A GRCh38
NC_000002.11:g.204732770C>A , CM000664.1:g.204732770C>A GRCh37
NC_000002.10:g.204441015C>A NCBI36
NG_011502.1:g.5262C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000696049.1:c.105C>A ENSP00000512353.1:p.Cys35Ter
ENST00000696479.1:c.177C>A ENSP00000512655.1:p.Cys59Ter
ENST00000648405.2:c.105C>A MANE Select ENSP00000497102.1:p.Cys35Ter
ENST00000295854.10:c.105C>A ENSP00000295854.6:p.Cys35Ter
ENST00000302823.7:c.105C>A ENSP00000303939.3:p.Cys35Ter
ENST00000472206.1:c.105C>A ENSP00000417779.1:p.Cys35Ter
ENST00000487393.1:n.105C>A
NM_001037631.2:c.105C>A NP_001032720.1:p.Cys35Ter
NM_005214.4:c.105C>A NP_005205.2:p.Cys35Ter
XR_241294.1:n.245C>A
NM_001037631.3:c.105C>A NP_001032720.1:p.Cys35Ter
NM_005214.5:c.105C>A MANE Select NP_005205.2:p.Cys35Ter