Canonical Allele Identifier: CA2495810601
Gene: EPCAM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47377028A= , CM000664.2:g.47377028A= GRCh38
NC_000002.11:g.47604167A= , CM000664.1:g.47604167A= GRCh37
NC_000002.10:g.47457671A= NCBI36
NG_012352.2:g.36866A= , LRG_215:g.36866A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263735.9:c.506A= MANE Select ENSP00000263735.4:p.Glu169=
ENST00000263735.8:c.506A= ENSP00000263735.4:p.Glu169=
ENST00000405271.5:c.590A= ENSP00000385476.1:p.Glu197=
ENST00000456133.5:c.590A= ENSP00000410675.1:p.Glu197=
ENST00000490733.1:n.355A=
NM_002354.2:c.506A= , LRG_215t1:c.506A= NP_002345.2:p.Glu169=
NM_002354.3:c.506A= MANE Select NP_002345.2:p.Glu169=