Canonical Allele Identifier: CA350138187

Gene: CTLA4

Linked Data

• ClinVar Variation Id: 430905
• ClinVar RCV Id: RCV000615288
• dbSNP Id: rs1553657387
• MyVariant Identifiers: chr2:g.204735359G>A (hg19) ; chr2:g.203870636G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203870636G>A , CM000664.2:g.203870636G>A	GRCh38
NC_000002.11:g.204735359G>A , CM000664.1:g.204735359G>A	GRCh37
NC_000002.10:g.204443604G>A	NCBI36
NG_011502.1:g.7851G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696049.1:c.160G>A	ENSP00000512353.1:p.Ala54Thr
ENST00000696479.1:c.232G>A	ENSP00000512655.1:p.Ala78Thr
ENST00000427473.3:n.194G>A
ENST00000648405.2:c.160G>A MANE Select	ENSP00000497102.1:p.Ala54Thr
ENST00000650075.1:n.184G>A
ENST00000295854.10:c.160G>A	ENSP00000295854.6:p.Ala54Thr
ENST00000302823.7:c.160G>A	ENSP00000303939.3:p.Ala54Thr
ENST00000427473.2:c.49G>A	ENSP00000409707.2:p.Ala17Thr
ENST00000472206.1:c.160G>A	ENSP00000417779.1:p.Ala54Thr
ENST00000487393.1:n.110-2072G>A
NM_001037631.2:c.160G>A	NP_001032720.1:p.Ala54Thr
NM_005214.4:c.160G>A	NP_005205.2:p.Ala54Thr
XR_241294.1:n.300G>A
NM_001037631.3:c.160G>A	NP_001032720.1:p.Ala54Thr
NM_005214.5:c.160G>A MANE Select	NP_005205.2:p.Ala54Thr