Canonical Allele Identifier: CA350137999

Gene: CTLA4

Linked Data

• MyVariant Identifiers: chr2:g.204732744T>G (hg19) ; chr2:g.203868021T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203868021T>G , CM000664.2:g.203868021T>G	GRCh38
NC_000002.11:g.204732744T>G , CM000664.1:g.204732744T>G	GRCh37
NC_000002.10:g.204440989T>G	NCBI36
NG_011502.1:g.5236T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000696049.1:c.79T>G	ENSP00000512353.1:p.Phe27Val
ENST00000696479.1:c.151T>G	ENSP00000512655.1:p.Phe51Val
ENST00000648405.2:c.79T>G MANE Select	ENSP00000497102.1:p.Phe27Val
ENST00000295854.10:c.79T>G	ENSP00000295854.6:p.Phe27Val
ENST00000302823.7:c.79T>G	ENSP00000303939.3:p.Phe27Val
ENST00000472206.1:c.79T>G	ENSP00000417779.1:p.Phe27Val
ENST00000487393.1:n.79T>G
NM_001037631.2:c.79T>G	NP_001032720.1:p.Phe27Val
NM_005214.4:c.79T>G	NP_005205.2:p.Phe27Val
XR_241294.1:n.219T>G
NM_001037631.3:c.79T>G	NP_001032720.1:p.Phe27Val
NM_005214.5:c.79T>G MANE Select	NP_005205.2:p.Phe27Val