Canonical Allele Identifier: CA350139103

Gene: CTLA4

Linked Data

• ClinVar Variation Id: 475279
• ClinVar RCV Id: RCV000558959
• dbSNP Id: rs1553657487
• MyVariant Identifiers: chr2:g.204736211G>A (hg19) ; chr2:g.203871488G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203871488G>A , CM000664.2:g.203871488G>A	GRCh38
NC_000002.11:g.204736211G>A , CM000664.1:g.204736211G>A	GRCh37
NC_000002.10:g.204444456G>A	NCBI36
NG_011502.1:g.8703G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696049.1:c.507+61G>A	ENSP00000512353.1:n.507+61G>A
ENST00000696479.1:c.639+1G>A	ENSP00000512655.1:n.639+1G>A
ENST00000427473.3:n.491+555G>A
ENST00000648405.2:c.567+1G>A MANE Select	ENSP00000497102.1:n.567+1G>A
ENST00000650075.1:n.591+1G>A
ENST00000295854.10:c.457+555G>A	ENSP00000295854.6:n.457+555G>A
ENST00000302823.7:c.567+1G>A	ENSP00000303939.3:n.567+1G>A
ENST00000427473.2:c.346+555G>A	ENSP00000409707.2:n.346+555G>A
ENST00000472206.1:c.172+840G>A	ENSP00000417779.1:n.172+840G>A
ENST00000487393.1:n.110-1220G>A
NM_001037631.2:c.457+555G>A	NP_001032720.1:n.457+555G>A
NM_005214.4:c.567+1G>A	NP_005205.2:n.567+1G>A
XR_241294.1:n.707+1G>A
NM_001037631.3:c.457+555G>A	NP_001032720.1:n.457+555G>A
NM_005214.5:c.567+1G>A MANE Select	NP_005205.2:n.567+1G>A