Canonical Allele Identifier: CA2495810680
Gene: EPCAM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47377183_47377184delinsAG , CM000664.2:g.47377183_47377184delinsAG GRCh38
NC_000002.11:g.47604322_47604323delinsAG , CM000664.1:g.47604322_47604323delinsAG GRCh37
NC_000002.10:g.47457826_47457827delinsAG NCBI36
NG_012352.2:g.37021_37022delinsAG , LRG_215:g.37021_37022delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000263735.9:c.555+106_555+107delinsAG MANE Select ENSP00000263735.4:n.555+106_555+107delinsAG
ENST00000263735.8:c.555+106_555+107delinsAG ENSP00000263735.4:n.555+106_555+107delinsAG
ENST00000405271.5:c.639+106_639+107delinsAG ENSP00000385476.1:n.639+106_639+107delinsAG
ENST00000456133.5:c.639+106_639+107delinsAG ENSP00000410675.1:n.639+106_639+107delinsAG
ENST00000490733.1:n.404+106_404+107delinsAG
NM_002354.2:c.555+106_555+107delinsAG , LRG_215t1:c.555+106_555+107delinsAG NP_002345.2:n.555+106_555+107delinsAG
NM_002354.3:c.555+106_555+107delinsAG MANE Select NP_002345.2:n.555+106_555+107delinsAG