Canonical Allele Identifier: CA431020688

Gene: CTLA4

Linked Data

• MyVariant Identifiers: chr2:g.204736198T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203871475T>A , CM000664.2:g.203871475T>A	GRCh38
NC_000002.11:g.204736198T>A , CM000664.1:g.204736198T>A	GRCh37
NC_000002.10:g.204444443T>A	NCBI36
NG_011502.1:g.8690T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696049.1:c.507+48T>A	ENSP00000512353.1:n.507+48T>A
ENST00000696479.1:c.627T>A	ENSP00000512655.1:p.Ser209=
ENST00000427473.3:n.491+542T>A
ENST00000648405.2:c.555T>A MANE Select	ENSP00000497102.1:p.Ser185=
ENST00000650075.1:n.579T>A
ENST00000295854.10:c.457+542T>A	ENSP00000295854.6:n.457+542T>A
ENST00000302823.7:c.555T>A	ENSP00000303939.3:p.Ser185=
ENST00000427473.2:c.346+542T>A	ENSP00000409707.2:n.346+542T>A
ENST00000472206.1:c.172+827T>A	ENSP00000417779.1:n.172+827T>A
ENST00000487393.1:n.110-1233T>A
NM_001037631.2:c.457+542T>A	NP_001032720.1:n.457+542T>A
NM_005214.4:c.555T>A	NP_005205.2:p.Ser185=
XR_241294.1:n.695T>A
NM_001037631.3:c.457+542T>A	NP_001032720.1:n.457+542T>A
NM_005214.5:c.555T>A MANE Select	NP_005205.2:p.Ser185=