Canonical Allele Identifier: CA2495810610
Gene: EPCAM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47377046A= , CM000664.2:g.47377046A= GRCh38
NC_000002.11:g.47604185A= , CM000664.1:g.47604185A= GRCh37
NC_000002.10:g.47457689A= NCBI36
NG_012352.2:g.36884A= , LRG_215:g.36884A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263735.9:c.524A= MANE Select ENSP00000263735.4:p.Gln175=
ENST00000263735.8:c.524A= ENSP00000263735.4:p.Gln175=
ENST00000405271.5:c.608A= ENSP00000385476.1:p.Gln203=
ENST00000456133.5:c.608A= ENSP00000410675.1:p.Gln203=
ENST00000490733.1:n.373A=
NM_002354.2:c.524A= , LRG_215t1:c.524A= NP_002345.2:p.Gln175=
NM_002354.3:c.524A= MANE Select NP_002345.2:p.Gln175=