Canonical Allele Identifier: CA2697551495

Gene: CTLA4

Linked Data

• ClinVar Variation Id: 2711876
• ClinVar RCV Id: RCV003586829

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203871492G>A , CM000664.2:g.203871492G>A	GRCh38
NC_000002.11:g.204736215G>A , CM000664.1:g.204736215G>A	GRCh37
NC_000002.10:g.204444460G>A	NCBI36
NG_011502.1:g.8707G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000696049.1:c.507+65G>A	ENSP00000512353.1:n.507+65G>A
ENST00000696479.1:c.639+5G>A	ENSP00000512655.1:n.639+5G>A
ENST00000427473.3:n.491+559G>A
ENST00000648405.2:c.567+5G>A MANE Select	ENSP00000497102.1:n.567+5G>A
ENST00000650075.1:n.591+5G>A
ENST00000295854.10:c.457+559G>A	ENSP00000295854.6:n.457+559G>A
ENST00000302823.7:c.567+5G>A	ENSP00000303939.3:n.567+5G>A
ENST00000427473.2:c.346+559G>A	ENSP00000409707.2:n.346+559G>A
ENST00000472206.1:c.172+844G>A	ENSP00000417779.1:n.172+844G>A
ENST00000487393.1:n.110-1216G>A
NM_001037631.2:c.457+559G>A	NP_001032720.1:n.457+559G>A
NM_005214.4:c.567+5G>A	NP_005205.2:n.567+5G>A
XR_241294.1:n.707+5G>A
NM_001037631.3:c.457+559G>A	NP_001032720.1:n.457+559G>A
NM_005214.5:c.567+5G>A MANE Select	NP_005205.2:n.567+5G>A