Canonical Allele Identifier: CA2495810620
Gene: EPCAM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47377073T= , CM000664.2:g.47377073T= GRCh38
NC_000002.11:g.47604212T= , CM000664.1:g.47604212T= GRCh37
NC_000002.10:g.47457716T= NCBI36
NG_012352.2:g.36911T= , LRG_215:g.36911T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263735.9:c.551T= MANE Select ENSP00000263735.4:p.Ile184=
ENST00000263735.8:c.551T= ENSP00000263735.4:p.Ile184=
ENST00000405271.5:c.635T= ENSP00000385476.1:p.Ile212=
ENST00000456133.5:c.635T= ENSP00000410675.1:p.Ile212=
ENST00000490733.1:n.400T=
NM_002354.2:c.551T= , LRG_215t1:c.551T= NP_002345.2:p.Ile184=
NM_002354.3:c.551T= MANE Select NP_002345.2:p.Ile184=