Canonical Allele Identifier: CA1322149058

Gene: CTLA4

Linked Data

• dbSNP Id: rs231778

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203869098G>C , CM000664.2:g.203869098G>C	GRCh38
NC_000002.11:g.204733821G>C , CM000664.1:g.204733821G>C	GRCh37
NC_000002.10:g.204442066G>C	NCBI36
NG_011502.1:g.6313G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000696049.1:c.109+1047G>C	ENSP00000512353.1:n.109+1047G>C
ENST00000696479.1:c.181+1047G>C	ENSP00000512655.1:n.181+1047G>C
ENST00000648405.2:c.109+1047G>C MANE Select	ENSP00000497102.1:n.109+1047G>C
ENST00000295854.10:c.109+1047G>C	ENSP00000295854.6:n.109+1047G>C
ENST00000302823.7:c.109+1047G>C	ENSP00000303939.3:n.109+1047G>C
ENST00000472206.1:c.109+1047G>C	ENSP00000417779.1:n.109+1047G>C
ENST00000487393.1:n.109+1047G>C
NM_001037631.2:c.109+1047G>C	NP_001032720.1:n.109+1047G>C
NM_005214.4:c.109+1047G>C	NP_005205.2:n.109+1047G>C
XR_241294.1:n.249+1047G>C
NM_001037631.3:c.109+1047G>C	NP_001032720.1:n.109+1047G>C
NM_005214.5:c.109+1047G>C MANE Select	NP_005205.2:n.109+1047G>C