Canonical Allele Identifier: CA2749800304

Gene: EPCAM

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47377243_47377244del , CM000664.2:g.47377243_47377244del	GRCh38
NC_000002.11:g.47604382_47604383del , CM000664.1:g.47604382_47604383del	GRCh37
NC_000002.10:g.47457886_47457887del	NCBI36
NG_012352.2:g.37081_37082del , LRG_215:g.37081_37082del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263735.9:c.555+166_555+167del MANE Select	ENSP00000263735.4:n.555+166_555+167del
ENST00000263735.8:c.555+166_555+167del	ENSP00000263735.4:n.555+166_555+167del
ENST00000405271.5:c.639+166_639+167del	ENSP00000385476.1:n.639+166_639+167del
ENST00000456133.5:c.639+166_639+167del	ENSP00000410675.1:n.639+166_639+167del
ENST00000490733.1:n.404+166_404+167del
NM_002354.2:c.555+166_555+167del , LRG_215t1:c.555+166_555+167del	NP_002345.2:n.555+166_555+167del
NM_002354.3:c.555+166_555+167del MANE Select	NP_002345.2:n.555+166_555+167del