Canonical Allele Identifier: CA350138919

Gene: CTLA4

Linked Data

• MyVariant Identifiers: chr2:g.204736128T>A (hg19) ; chr2:g.203871405T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203871405T>A , CM000664.2:g.203871405T>A	GRCh38
NC_000002.11:g.204736128T>A , CM000664.1:g.204736128T>A	GRCh37
NC_000002.10:g.204444373T>A	NCBI36
NG_011502.1:g.8620T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000696049.1:c.485T>A	ENSP00000512353.1:p.Phe162Tyr
ENST00000696479.1:c.557T>A	ENSP00000512655.1:p.Phe186Tyr
ENST00000427473.3:n.491+472T>A
ENST00000648405.2:c.485T>A MANE Select	ENSP00000497102.1:p.Phe162Tyr
ENST00000650075.1:n.509T>A
ENST00000295854.10:c.457+472T>A	ENSP00000295854.6:n.457+472T>A
ENST00000302823.7:c.485T>A	ENSP00000303939.3:p.Phe162Tyr
ENST00000427473.2:c.346+472T>A	ENSP00000409707.2:n.346+472T>A
ENST00000472206.1:c.172+757T>A	ENSP00000417779.1:n.172+757T>A
ENST00000487393.1:n.110-1303T>A
NM_001037631.2:c.457+472T>A	NP_001032720.1:n.457+472T>A
NM_005214.4:c.485T>A	NP_005205.2:p.Phe162Tyr
XR_241294.1:n.625T>A
NM_001037631.3:c.457+472T>A	NP_001032720.1:n.457+472T>A
NM_005214.5:c.485T>A MANE Select	NP_005205.2:p.Phe162Tyr