Canonical Allele Identifier: CA2662768901

Gene: CTLA4

Linked Data

• gnomAD v4: 2-203871587-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203871587A>G , CM000664.2:g.203871587A>G	GRCh38
NC_000002.11:g.204736310A>G , CM000664.1:g.204736310A>G	GRCh37
NC_000002.10:g.204444555A>G	NCBI36
NG_011502.1:g.8802A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696049.1:c.507+160A>G	ENSP00000512353.1:n.507+160A>G
ENST00000696479.1:c.639+100A>G	ENSP00000512655.1:n.639+100A>G
ENST00000427473.3:n.491+654A>G
ENST00000648405.2:c.567+100A>G MANE Select	ENSP00000497102.1:n.567+100A>G
ENST00000650075.1:n.591+100A>G
ENST00000295854.10:c.457+654A>G	ENSP00000295854.6:n.457+654A>G
ENST00000302823.7:c.567+100A>G	ENSP00000303939.3:n.567+100A>G
ENST00000427473.2:c.346+654A>G	ENSP00000409707.2:n.346+654A>G
ENST00000472206.1:c.172+939A>G	ENSP00000417779.1:n.172+939A>G
ENST00000487393.1:n.110-1121A>G
NM_001037631.2:c.457+654A>G	NP_001032720.1:n.457+654A>G
NM_005214.4:c.567+100A>G	NP_005205.2:n.567+100A>G
XR_241294.1:n.707+100A>G
NM_001037631.3:c.457+654A>G	NP_001032720.1:n.457+654A>G
NM_005214.5:c.567+100A>G MANE Select	NP_005205.2:n.567+100A>G