Canonical Allele Identifier: CA431020593

Gene: CTLA4

Linked Data

• gnomAD v4: 2-203871439-G-T
• MyVariant Identifiers: chr2:g.204736162G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203871439G>T , CM000664.2:g.203871439G>T	GRCh38
NC_000002.11:g.204736162G>T , CM000664.1:g.204736162G>T	GRCh37
NC_000002.10:g.204444407G>T	NCBI36
NG_011502.1:g.8654G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696049.1:c.507+12G>T	ENSP00000512353.1:n.507+12G>T
ENST00000696479.1:c.591G>T	ENSP00000512655.1:p.Gly197=
ENST00000427473.3:n.491+506G>T
ENST00000648405.2:c.519G>T MANE Select	ENSP00000497102.1:p.Gly173=
ENST00000650075.1:n.543G>T
ENST00000295854.10:c.457+506G>T	ENSP00000295854.6:n.457+506G>T
ENST00000302823.7:c.519G>T	ENSP00000303939.3:p.Gly173=
ENST00000427473.2:c.346+506G>T	ENSP00000409707.2:n.346+506G>T
ENST00000472206.1:c.172+791G>T	ENSP00000417779.1:n.172+791G>T
ENST00000487393.1:n.110-1269G>T
NM_001037631.2:c.457+506G>T	NP_001032720.1:n.457+506G>T
NM_005214.4:c.519G>T	NP_005205.2:p.Gly173=
XR_241294.1:n.659G>T
NM_001037631.3:c.457+506G>T	NP_001032720.1:n.457+506G>T
NM_005214.5:c.519G>T MANE Select	NP_005205.2:p.Gly173=