Canonical Allele Identifier: CA2495810599
Gene: EPCAM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47377023G= , CM000664.2:g.47377023G= GRCh38
NC_000002.11:g.47604162G= , CM000664.1:g.47604162G= GRCh37
NC_000002.10:g.47457666G= NCBI36
NG_012352.2:g.36861G= , LRG_215:g.36861G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263735.9:c.501G= MANE Select ENSP00000263735.4:p.Gln167=
ENST00000263735.8:c.501G= ENSP00000263735.4:p.Gln167=
ENST00000405271.5:c.585G= ENSP00000385476.1:p.Gln195=
ENST00000456133.5:c.585G= ENSP00000410675.1:p.Gln195=
ENST00000490733.1:n.350G=
NM_002354.2:c.501G= , LRG_215t1:c.501G= NP_002345.2:p.Gln167=
NM_002354.3:c.501G= MANE Select NP_002345.2:p.Gln167=