Canonical Allele Identifier: CA425947354
Gene: EPCAM HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.47604168G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47377029G>A , CM000664.2:g.47377029G>A GRCh38
NC_000002.11:g.47604168G>A , CM000664.1:g.47604168G>A GRCh37
NC_000002.10:g.47457672G>A NCBI36
NG_012352.2:g.36867G>A , LRG_215:g.36867G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000263735.9:c.507G>A MANE Select ENSP00000263735.4:p.Glu169=
ENST00000263735.8:c.507G>A ENSP00000263735.4:p.Glu169=
ENST00000405271.5:c.591G>A ENSP00000385476.1:p.Glu197=
ENST00000456133.5:c.591G>A ENSP00000410675.1:p.Glu197=
ENST00000490733.1:n.356G>A
NM_002354.2:c.507G>A , LRG_215t1:c.507G>A NP_002345.2:p.Glu169=
NM_002354.3:c.507G>A MANE Select NP_002345.2:p.Glu169=