Canonical Allele Identifier: CA1041459790

Gene: CTLA4

Linked Data

• dbSNP Id: rs1688725726
• gnomAD v3: 2-203871219-A-T
• gnomAD v4: 2-203871219-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203871219A>T , CM000664.2:g.203871219A>T	GRCh38
NC_000002.11:g.204735942A>T , CM000664.1:g.204735942A>T	GRCh37
NC_000002.10:g.204444187A>T	NCBI36
NG_011502.1:g.8434A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696049.1:c.458-159A>T	ENSP00000512353.1:n.458-159A>T
ENST00000696479.1:c.530-159A>T	ENSP00000512655.1:n.530-159A>T
ENST00000427473.3:n.491+286A>T
ENST00000648405.2:c.458-159A>T MANE Select	ENSP00000497102.1:n.458-159A>T
ENST00000650075.1:n.482-159A>T
ENST00000295854.10:c.457+286A>T	ENSP00000295854.6:n.457+286A>T
ENST00000302823.7:c.458-159A>T	ENSP00000303939.3:n.458-159A>T
ENST00000427473.2:c.346+286A>T	ENSP00000409707.2:n.346+286A>T
ENST00000472206.1:c.172+571A>T	ENSP00000417779.1:n.172+571A>T
ENST00000487393.1:n.110-1489A>T
NM_001037631.2:c.457+286A>T	NP_001032720.1:n.457+286A>T
NM_005214.4:c.458-159A>T	NP_005205.2:n.458-159A>T
XR_241294.1:n.598-159A>T
NM_001037631.3:c.457+286A>T	NP_001032720.1:n.457+286A>T
NM_005214.5:c.458-159A>T MANE Select	NP_005205.2:n.458-159A>T