Canonical Allele Identifier: CA350138892

Gene: CTLA4

Linked Data

• ClinVar Variation Id: 3032071
• ClinVar RCV Id: RCV003899805
• dbSNP Id: rs1688729782
• gnomAD v4: 2-203871392-C-T
• COSMIC: COSM222747
• MyVariant Identifiers: chr2:g.204736115C>T (hg19) ; chr2:g.203871392C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203871392C>T , CM000664.2:g.203871392C>T	GRCh38
NC_000002.11:g.204736115C>T , CM000664.1:g.204736115C>T	GRCh37
NC_000002.10:g.204444360C>T	NCBI36
NG_011502.1:g.8607C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696049.1:c.472C>T	ENSP00000512353.1:p.Pro158Ser
ENST00000696479.1:c.544C>T	ENSP00000512655.1:p.Pro182Ser
ENST00000427473.3:n.491+459C>T
ENST00000648405.2:c.472C>T MANE Select	ENSP00000497102.1:p.Pro158Ser
ENST00000650075.1:n.496C>T
ENST00000295854.10:c.457+459C>T	ENSP00000295854.6:n.457+459C>T
ENST00000302823.7:c.472C>T	ENSP00000303939.3:p.Pro158Ser
ENST00000427473.2:c.346+459C>T	ENSP00000409707.2:n.346+459C>T
ENST00000472206.1:c.172+744C>T	ENSP00000417779.1:n.172+744C>T
ENST00000487393.1:n.110-1316C>T
NM_001037631.2:c.457+459C>T	NP_001032720.1:n.457+459C>T
NM_005214.4:c.472C>T	NP_005205.2:p.Pro158Ser
XR_241294.1:n.612C>T
NM_001037631.3:c.457+459C>T	NP_001032720.1:n.457+459C>T
NM_005214.5:c.472C>T MANE Select	NP_005205.2:p.Pro158Ser