Canonical Allele Identifier: CA763553488

Gene: CTLA4

Linked Data

• dbSNP Id: rs1239393475
• MyVariant Identifiers: chr2:g.204734116_204734118del (hg19) ; chr2:g.203869393_203869395del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203869393_203869395del , CM000664.2:g.203869393_203869395del	GRCh38
NC_000002.11:g.204734116_204734118del , CM000664.1:g.204734116_204734118del	GRCh37
NC_000002.10:g.204442361_204442363del	NCBI36
NG_011502.1:g.6608_6610del

Transcript Alleles

HGVS	Amino-acid change
ENST00000696049.1:c.110-1193_110-1191del	ENSP00000512353.1:n.110-1193_110-1191del
ENST00000696479.1:c.182-1193_182-1191del	ENSP00000512655.1:n.182-1193_182-1191del
ENST00000648405.2:c.110-1193_110-1191del MANE Select	ENSP00000497102.1:n.110-1193_110-1191del
ENST00000295854.10:c.110-1193_110-1191del	ENSP00000295854.6:n.110-1193_110-1191del
ENST00000302823.7:c.110-1193_110-1191del	ENSP00000303939.3:n.110-1193_110-1191del
ENST00000472206.1:c.110-1193_110-1191del	ENSP00000417779.1:n.110-1193_110-1191del
ENST00000487393.1:n.109+1342_109+1344del
NM_001037631.2:c.110-1193_110-1191del	NP_001032720.1:n.110-1193_110-1191del
NM_005214.4:c.110-1193_110-1191del	NP_005205.2:n.110-1193_110-1191del
XR_241294.1:n.250-1193_250-1191del
NM_001037631.3:c.110-1193_110-1191del	NP_001032720.1:n.110-1193_110-1191del
NM_005214.5:c.110-1193_110-1191del MANE Select	NP_005205.2:n.110-1193_110-1191del