Canonical Allele Identifier: CA350138953

Gene: CTLA4

Linked Data

• MyVariant Identifiers: chr2:g.204736142C>T (hg19) ; chr2:g.203871419C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203871419C>T , CM000664.2:g.203871419C>T	GRCh38
NC_000002.11:g.204736142C>T , CM000664.1:g.204736142C>T	GRCh37
NC_000002.10:g.204444387C>T	NCBI36
NG_011502.1:g.8634C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696049.1:c.499C>T	ENSP00000512353.1:p.Leu167Phe
ENST00000696479.1:c.571C>T	ENSP00000512655.1:p.Leu191Phe
ENST00000427473.3:n.491+486C>T
ENST00000648405.2:c.499C>T MANE Select	ENSP00000497102.1:p.Leu167Phe
ENST00000650075.1:n.523C>T
ENST00000295854.10:c.457+486C>T	ENSP00000295854.6:n.457+486C>T
ENST00000302823.7:c.499C>T	ENSP00000303939.3:p.Leu167Phe
ENST00000427473.2:c.346+486C>T	ENSP00000409707.2:n.346+486C>T
ENST00000472206.1:c.172+771C>T	ENSP00000417779.1:n.172+771C>T
ENST00000487393.1:n.110-1289C>T
NM_001037631.2:c.457+486C>T	NP_001032720.1:n.457+486C>T
NM_005214.4:c.499C>T	NP_005205.2:p.Leu167Phe
XR_241294.1:n.639C>T
NM_001037631.3:c.457+486C>T	NP_001032720.1:n.457+486C>T
NM_005214.5:c.499C>T MANE Select	NP_005205.2:p.Leu167Phe