Canonical Allele Identifier: CA431020361

Gene: CTLA4

Linked Data

• gnomAD v4: 2-203868008-C-T
• MyVariant Identifiers: chr2:g.204732731C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203868008C>T , CM000664.2:g.203868008C>T	GRCh38
NC_000002.11:g.204732731C>T , CM000664.1:g.204732731C>T	GRCh37
NC_000002.10:g.204440976C>T	NCBI36
NG_011502.1:g.5223C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000696049.1:c.66C>T	ENSP00000512353.1:p.Cys22=
ENST00000696479.1:c.138C>T	ENSP00000512655.1:p.Cys46=
ENST00000648405.2:c.66C>T MANE Select	ENSP00000497102.1:p.Cys22=
ENST00000295854.10:c.66C>T	ENSP00000295854.6:p.Cys22=
ENST00000302823.7:c.66C>T	ENSP00000303939.3:p.Cys22=
ENST00000472206.1:c.66C>T	ENSP00000417779.1:p.Cys22=
ENST00000487393.1:n.66C>T
NM_001037631.2:c.66C>T	NP_001032720.1:p.Cys22=
NM_005214.4:c.66C>T	NP_005205.2:p.Cys22=
XR_241294.1:n.206C>T
NM_001037631.3:c.66C>T	NP_001032720.1:p.Cys22=
NM_005214.5:c.66C>T MANE Select	NP_005205.2:p.Cys22=