Canonical Allele Identifier: CA173995
Gene: CTLA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 161111
ClinVar RCV Id: RCV000148292
dbSNP Id: rs606231419

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203871492G>C , CM000664.2:g.203871492G>C GRCh38
NC_000002.11:g.204736215G>C , CM000664.1:g.204736215G>C GRCh37
NC_000002.10:g.204444460G>C NCBI36
NG_011502.1:g.8707G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000696049.1:c.507+65G>C ENSP00000512353.1:n.507+65G>C
ENST00000696479.1:c.639+5G>C ENSP00000512655.1:n.639+5G>C
ENST00000427473.3:n.491+559G>C
ENST00000648405.2:c.567+5G>C MANE Select ENSP00000497102.1:n.567+5G>C
ENST00000650075.1:n.591+5G>C
ENST00000295854.10:c.457+559G>C ENSP00000295854.6:n.457+559G>C
ENST00000302823.7:c.567+5G>C ENSP00000303939.3:n.567+5G>C
ENST00000427473.2:c.346+559G>C ENSP00000409707.2:n.346+559G>C
ENST00000472206.1:c.172+844G>C ENSP00000417779.1:n.172+844G>C
ENST00000487393.1:n.110-1216G>C
NM_001037631.2:c.457+559G>C NP_001032720.1:n.457+559G>C
NM_005214.4:c.567+5G>C NP_005205.2:n.567+5G>C
XR_241294.1:n.707+5G>C
NM_001037631.3:c.457+559G>C NP_001032720.1:n.457+559G>C
NM_005214.5:c.567+5G>C MANE Select NP_005205.2:n.567+5G>C