Canonical Allele Identifier: CA350138182

Gene: CTLA4

Linked Data

• MyVariant Identifiers: chr2:g.204735357T>C (hg19) ; chr2:g.203870634T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203870634T>C , CM000664.2:g.203870634T>C	GRCh38
NC_000002.11:g.204735357T>C , CM000664.1:g.204735357T>C	GRCh37
NC_000002.10:g.204443602T>C	NCBI36
NG_011502.1:g.7849T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000696049.1:c.158T>C	ENSP00000512353.1:p.Ile53Thr
ENST00000696479.1:c.230T>C	ENSP00000512655.1:p.Ile77Thr
ENST00000427473.3:n.192T>C
ENST00000648405.2:c.158T>C MANE Select	ENSP00000497102.1:p.Ile53Thr
ENST00000650075.1:n.182T>C
ENST00000295854.10:c.158T>C	ENSP00000295854.6:p.Ile53Thr
ENST00000302823.7:c.158T>C	ENSP00000303939.3:p.Ile53Thr
ENST00000427473.2:c.47T>C	ENSP00000409707.2:p.Ile16Thr
ENST00000472206.1:c.158T>C	ENSP00000417779.1:p.Ile53Thr
ENST00000487393.1:n.110-2074T>C
NM_001037631.2:c.158T>C	NP_001032720.1:p.Ile53Thr
NM_005214.4:c.158T>C	NP_005205.2:p.Ile53Thr
XR_241294.1:n.298T>C
NM_001037631.3:c.158T>C	NP_001032720.1:p.Ile53Thr
NM_005214.5:c.158T>C MANE Select	NP_005205.2:p.Ile53Thr