Canonical Allele Identifier: CA2495810609
Gene: EPCAM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47377045C= , CM000664.2:g.47377045C= GRCh38
NC_000002.11:g.47604184C= , CM000664.1:g.47604184C= GRCh37
NC_000002.10:g.47457688C= NCBI36
NG_012352.2:g.36883C= , LRG_215:g.36883C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263735.9:c.523C= MANE Select ENSP00000263735.4:p.Gln175=
ENST00000263735.8:c.523C= ENSP00000263735.4:p.Gln175=
ENST00000405271.5:c.607C= ENSP00000385476.1:p.Gln203=
ENST00000456133.5:c.607C= ENSP00000410675.1:p.Gln203=
ENST00000490733.1:n.372C=
NM_002354.2:c.523C= , LRG_215t1:c.523C= NP_002345.2:p.Gln175=
NM_002354.3:c.523C= MANE Select NP_002345.2:p.Gln175=