Canonical Allele Identifier: CA1322149109

Gene: CTLA4

Linked Data

• dbSNP Id: rs1688684873

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203869235G>A , CM000664.2:g.203869235G>A	GRCh38
NC_000002.11:g.204733958G>A , CM000664.1:g.204733958G>A	GRCh37
NC_000002.10:g.204442203G>A	NCBI36
NG_011502.1:g.6450G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000696049.1:c.109+1184G>A	ENSP00000512353.1:n.109+1184G>A
ENST00000696479.1:c.181+1184G>A	ENSP00000512655.1:n.181+1184G>A
ENST00000648405.2:c.109+1184G>A MANE Select	ENSP00000497102.1:n.109+1184G>A
ENST00000295854.10:c.109+1184G>A	ENSP00000295854.6:n.109+1184G>A
ENST00000302823.7:c.109+1184G>A	ENSP00000303939.3:n.109+1184G>A
ENST00000472206.1:c.109+1184G>A	ENSP00000417779.1:n.109+1184G>A
ENST00000487393.1:n.109+1184G>A
NM_001037631.2:c.109+1184G>A	NP_001032720.1:n.109+1184G>A
NM_005214.4:c.109+1184G>A	NP_005205.2:n.109+1184G>A
XR_241294.1:n.249+1184G>A
NM_001037631.3:c.109+1184G>A	NP_001032720.1:n.109+1184G>A
NM_005214.5:c.109+1184G>A MANE Select	NP_005205.2:n.109+1184G>A