Canonical Allele Identifier: CA2576960555
Gene: EPCAM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47377103del , CM000664.2:g.47377103del GRCh38
NC_000002.11:g.47604242del , CM000664.1:g.47604242del GRCh37
NC_000002.10:g.47457746del NCBI36
NG_012352.2:g.36941del , LRG_215:g.36941del

Transcript Alleles

HGVS Amino-acid Change
ENST00000263735.9:c.555+26del MANE Select ENSP00000263735.4:n.555+26del
ENST00000263735.8:c.555+26del ENSP00000263735.4:n.555+26del
ENST00000405271.5:c.639+26del ENSP00000385476.1:n.639+26del
ENST00000456133.5:c.639+26del ENSP00000410675.1:n.639+26del
ENST00000490733.1:n.404+26del
NM_002354.2:c.555+26del , LRG_215t1:c.555+26del NP_002345.2:n.555+26del
NM_002354.3:c.555+26del MANE Select NP_002345.2:n.555+26del