Canonical Allele Identifier: CA916756440
Gene: CTLA4 HGNC NCBI

Linked Data

dbSNP Id: rs1581572716

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203869360_203869361insCA , CM000664.2:g.203869360_203869361insCA GRCh38
NC_000002.11:g.204734083_204734084insCA , CM000664.1:g.204734083_204734084insCA GRCh37
NC_000002.10:g.204442328_204442329insCA NCBI36
NG_011502.1:g.6575_6576insCA

Transcript Alleles

HGVS Amino-acid change
ENST00000696049.1:c.110-1226_110-1225insCA ENSP00000512353.1:n.110-1226_110-1225insC...
ENST00000696479.1:c.182-1226_182-1225insCA ENSP00000512655.1:n.182-1226_182-1225insC...
ENST00000648405.2:c.110-1226_110-1225insCA MANE Select ENSP00000497102.1:n.110-1226_110-1225insC...
ENST00000295854.10:c.110-1226_110-1225insCA ENSP00000295854.6:n.110-1226_110-1225insC...
ENST00000302823.7:c.110-1226_110-1225insCA ENSP00000303939.3:n.110-1226_110-1225insC...
ENST00000472206.1:c.110-1226_110-1225insCA ENSP00000417779.1:n.110-1226_110-1225insC...
ENST00000487393.1:n.109+1309_109+1310insCA
NM_001037631.2:c.110-1226_110-1225insCA NP_001032720.1:n.110-1226_110-1225insCA
NM_005214.4:c.110-1226_110-1225insCA NP_005205.2:n.110-1226_110-1225insCA
XR_241294.1:n.250-1226_250-1225insCA
NM_001037631.3:c.110-1226_110-1225insCA NP_001032720.1:n.110-1226_110-1225insCA
NM_005214.5:c.110-1226_110-1225insCA MANE Select NP_005205.2:n.110-1226_110-1225insCA