Canonical Allele Identifier: CA350138170

Gene: CTLA4

Linked Data

• MyVariant Identifiers: chr2:g.204735351G>T (hg19) ; chr2:g.203870628G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203870628G>T , CM000664.2:g.203870628G>T	GRCh38
NC_000002.11:g.204735351G>T , CM000664.1:g.204735351G>T	GRCh37
NC_000002.10:g.204443596G>T	NCBI36
NG_011502.1:g.7843G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000696049.1:c.152G>T	ENSP00000512353.1:p.Arg51Leu
ENST00000696479.1:c.224G>T	ENSP00000512655.1:p.Arg75Leu
ENST00000427473.3:n.186G>T
ENST00000648405.2:c.152G>T MANE Select	ENSP00000497102.1:p.Arg51Leu
ENST00000650075.1:n.176G>T
ENST00000295854.10:c.152G>T	ENSP00000295854.6:p.Arg51Leu
ENST00000302823.7:c.152G>T	ENSP00000303939.3:p.Arg51Leu
ENST00000427473.2:c.41G>T	ENSP00000409707.2:p.Arg14Leu
ENST00000472206.1:c.152G>T	ENSP00000417779.1:p.Arg51Leu
ENST00000487393.1:n.110-2080G>T
NM_001037631.2:c.152G>T	NP_001032720.1:p.Arg51Leu
NM_005214.4:c.152G>T	NP_005205.2:p.Arg51Leu
XR_241294.1:n.292G>T
NM_001037631.3:c.152G>T	NP_001032720.1:p.Arg51Leu
NM_005214.5:c.152G>T MANE Select	NP_005205.2:p.Arg51Leu