Canonical Allele Identifier: CA16124052

Gene: CTLA4

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203868865T>C , CM000664.2:g.203868865T>C	GRCh38
NC_000002.11:g.204733588T>C , CM000664.1:g.204733588T>C	GRCh37
NC_000002.10:g.204441833T>C	NCBI36
NG_011502.1:g.6080T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696049.1:c.109+814T>C	ENSP00000512353.1:n.109+814T>C
ENST00000696479.1:c.181+814T>C	ENSP00000512655.1:n.181+814T>C
ENST00000648405.2:c.109+814T>C MANE Select	ENSP00000497102.1:n.109+814T>C
ENST00000295854.10:c.109+814T>C	ENSP00000295854.6:n.109+814T>C
ENST00000302823.7:c.109+814T>C	ENSP00000303939.3:n.109+814T>C
ENST00000472206.1:c.109+814T>C	ENSP00000417779.1:n.109+814T>C
ENST00000487393.1:n.109+814T>C
NM_001037631.2:c.109+814T>C	NP_001032720.1:n.109+814T>C
NM_005214.4:c.109+814T>C	NP_005205.2:n.109+814T>C
XR_241294.1:n.249+814T>C
NM_001037631.3:c.109+814T>C	NP_001032720.1:n.109+814T>C
NM_005214.5:c.109+814T>C MANE Select	NP_005205.2:n.109+814T>C