Canonical Allele Identifier: CA431122402

Gene: CTLA4

Linked Data

• MyVariant Identifiers: chr2:g.204735361C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203870638C>A , CM000664.2:g.203870638C>A	GRCh38
NC_000002.11:g.204735361C>A , CM000664.1:g.204735361C>A	GRCh37
NC_000002.10:g.204443606C>A	NCBI36
NG_011502.1:g.7853C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000696049.1:c.162C>A	ENSP00000512353.1:p.Ala54=
ENST00000696479.1:c.234C>A	ENSP00000512655.1:p.Ala78=
ENST00000427473.3:n.196C>A
ENST00000648405.2:c.162C>A MANE Select	ENSP00000497102.1:p.Ala54=
ENST00000650075.1:n.186C>A
ENST00000295854.10:c.162C>A	ENSP00000295854.6:p.Ala54=
ENST00000302823.7:c.162C>A	ENSP00000303939.3:p.Ala54=
ENST00000427473.2:c.51C>A	ENSP00000409707.2:p.Ala17=
ENST00000472206.1:c.162C>A	ENSP00000417779.1:p.Ala54=
ENST00000487393.1:n.110-2070C>A
NM_001037631.2:c.162C>A	NP_001032720.1:p.Ala54=
NM_005214.4:c.162C>A	NP_005205.2:p.Ala54=
XR_241294.1:n.302C>A
NM_001037631.3:c.162C>A	NP_001032720.1:p.Ala54=
NM_005214.5:c.162C>A MANE Select	NP_005205.2:p.Ala54=