Canonical Allele Identifier: CA2577220042
Gene: CTLA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203867922del , CM000664.2:g.203867922del GRCh38
NC_000002.11:g.204732645del , CM000664.1:g.204732645del GRCh37
NC_000002.10:g.204440890del NCBI36
NG_011502.1:g.5137del

Transcript Alleles

HGVS Amino-acid change
ENST00000696049.1:c.-21del ENSP00000512353.1:n.-21del
ENST00000696479.1:c.52del ENSP00000512655.1:p.Glu18AsnfsTer20
ENST00000648405.2:c.-21del MANE Select ENSP00000497102.1:n.-21del
ENST00000302823.7:c.-21del ENSP00000303939.3:n.-21del
NM_001037631.2:c.-21del NP_001032720.1:n.-21del
NM_005214.4:c.-21del NP_005205.2:n.-21del
XR_241294.1:n.120del
NM_001037631.3:c.-21del NP_001032720.1:n.-21del
NM_005214.5:c.-21del MANE Select NP_005205.2:n.-21del