Canonical Allele Identifier: CA350138875

Gene: CTLA4

Linked Data

• gnomAD v4: 2-203871385-A-C
• MyVariant Identifiers: chr2:g.204736108A>C (hg19) ; chr2:g.203871385A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203871385A>C , CM000664.2:g.203871385A>C	GRCh38
NC_000002.11:g.204736108A>C , CM000664.1:g.204736108A>C	GRCh37
NC_000002.10:g.204444353A>C	NCBI36
NG_011502.1:g.8600A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696049.1:c.465A>C	ENSP00000512353.1:p.Glu155Asp
ENST00000696479.1:c.537A>C	ENSP00000512655.1:p.Glu179Asp
ENST00000427473.3:n.491+452A>C
ENST00000648405.2:c.465A>C MANE Select	ENSP00000497102.1:p.Glu155Asp
ENST00000650075.1:n.489A>C
ENST00000295854.10:c.457+452A>C	ENSP00000295854.6:n.457+452A>C
ENST00000302823.7:c.465A>C	ENSP00000303939.3:p.Glu155Asp
ENST00000427473.2:c.346+452A>C	ENSP00000409707.2:n.346+452A>C
ENST00000472206.1:c.172+737A>C	ENSP00000417779.1:n.172+737A>C
ENST00000487393.1:n.110-1323A>C
NM_001037631.2:c.457+452A>C	NP_001032720.1:n.457+452A>C
NM_005214.4:c.465A>C	NP_005205.2:p.Glu155Asp
XR_241294.1:n.605A>C
NM_001037631.3:c.457+452A>C	NP_001032720.1:n.457+452A>C
NM_005214.5:c.465A>C MANE Select	NP_005205.2:p.Glu155Asp