Canonical Allele Identifier: CA350139028

Gene: CTLA4

Linked Data

• dbSNP Id: rs1581574347
• MyVariant Identifiers: chr2:g.204736176G>C (hg19) ; chr2:g.203871453G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203871453G>C , CM000664.2:g.203871453G>C	GRCh38
NC_000002.11:g.204736176G>C , CM000664.1:g.204736176G>C	GRCh37
NC_000002.10:g.204444421G>C	NCBI36
NG_011502.1:g.8668G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696049.1:c.507+26G>C	ENSP00000512353.1:n.507+26G>C
ENST00000696479.1:c.605G>C	ENSP00000512655.1:p.Ser202Thr
ENST00000427473.3:n.491+520G>C
ENST00000648405.2:c.533G>C MANE Select	ENSP00000497102.1:p.Ser178Thr
ENST00000650075.1:n.557G>C
ENST00000295854.10:c.457+520G>C	ENSP00000295854.6:n.457+520G>C
ENST00000302823.7:c.533G>C	ENSP00000303939.3:p.Ser178Thr
ENST00000427473.2:c.346+520G>C	ENSP00000409707.2:n.346+520G>C
ENST00000472206.1:c.172+805G>C	ENSP00000417779.1:n.172+805G>C
ENST00000487393.1:n.110-1255G>C
NM_001037631.2:c.457+520G>C	NP_001032720.1:n.457+520G>C
NM_005214.4:c.533G>C	NP_005205.2:p.Ser178Thr
XR_241294.1:n.673G>C
NM_001037631.3:c.457+520G>C	NP_001032720.1:n.457+520G>C
NM_005214.5:c.533G>C MANE Select	NP_005205.2:p.Ser178Thr