Canonical Allele Identifier: CA350139053

Gene: CTLA4

Linked Data

• MyVariant Identifiers: chr2:g.204736187A>G (hg19) ; chr2:g.203871464A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203871464A>G , CM000664.2:g.203871464A>G	GRCh38
NC_000002.11:g.204736187A>G , CM000664.1:g.204736187A>G	GRCh37
NC_000002.10:g.204444432A>G	NCBI36
NG_011502.1:g.8679A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696049.1:c.507+37A>G	ENSP00000512353.1:n.507+37A>G
ENST00000696479.1:c.616A>G	ENSP00000512655.1:p.Thr206Ala
ENST00000427473.3:n.491+531A>G
ENST00000648405.2:c.544A>G MANE Select	ENSP00000497102.1:p.Thr182Ala
ENST00000650075.1:n.568A>G
ENST00000295854.10:c.457+531A>G	ENSP00000295854.6:n.457+531A>G
ENST00000302823.7:c.544A>G	ENSP00000303939.3:p.Thr182Ala
ENST00000427473.2:c.346+531A>G	ENSP00000409707.2:n.346+531A>G
ENST00000472206.1:c.172+816A>G	ENSP00000417779.1:n.172+816A>G
ENST00000487393.1:n.110-1244A>G
NM_001037631.2:c.457+531A>G	NP_001032720.1:n.457+531A>G
NM_005214.4:c.544A>G	NP_005205.2:p.Thr182Ala
XR_241294.1:n.684A>G
NM_001037631.3:c.457+531A>G	NP_001032720.1:n.457+531A>G
NM_005214.5:c.544A>G MANE Select	NP_005205.2:p.Thr182Ala