Canonical Allele Identifier: CA2749800298
Gene: EPCAM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47377194_47377195insACATTAA , CM000664.2:g.47377194_47377195insACATTAA GRCh38
NC_000002.11:g.47604333_47604334insACATTAA , CM000664.1:g.47604333_47604334insACATTAA GRCh37
NC_000002.10:g.47457837_47457838insACATTAA NCBI36
NG_012352.2:g.37032_37033insACATTAA , LRG_215:g.37032_37033insACATTAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000263735.9:c.555+117_555+118insACATTAA MANE Select ENSP00000263735.4:n.555+117_555+118insACATTAA
ENST00000263735.8:c.555+117_555+118insACATTAA ENSP00000263735.4:n.555+117_555+118insACATTAA
ENST00000405271.5:c.639+117_639+118insACATTAA ENSP00000385476.1:n.639+117_639+118insACATTAA
ENST00000456133.5:c.639+117_639+118insACATTAA ENSP00000410675.1:n.639+117_639+118insACATTAA
ENST00000490733.1:n.404+117_404+118insACATTAA
NM_002354.2:c.555+117_555+118insACATTAA , LRG_215t1:c.555+117_555+118insACATTAA NP_002345.2:n.555+117_555+118insACATTAA
NM_002354.3:c.555+117_555+118insACATTAA MANE Select NP_002345.2:n.555+117_555+118insACATTAA