Canonical Allele Identifier: CA346722522
Gene: EPCAM HGNC NCBI
MyVariant.info:
Revel Score:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47373519C>A , CM000664.2:g.47373519C>A GRCh38
NC_000002.11:g.47600658C>A , CM000664.1:g.47600658C>A GRCh37
NC_000002.10:g.47454162C>A NCBI36
NG_012352.2:g.33357C>A , LRG_215:g.33357C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000263735.9:c.133C>A MANE Select ENSP00000263735.4:p.Gln45Lys
ENST00000263735.8:c.133C>A ENSP00000263735.4:p.Gln45Lys
ENST00000405271.5:c.217C>A ENSP00000385476.1:p.Gln73Lys
ENST00000419334.1:c.361C>A ENSP00000389028.1:p.Gln121Lys
ENST00000456133.5:c.217C>A ENSP00000410675.1:p.Gln73Lys
ENST00000474691.1:n.164C>A
NM_002354.2:c.133C>A , LRG_215t1:c.133C>A NP_002345.2:p.Gln45Lys
NM_002354.3:c.133C>A MANE Select NP_002345.2:p.Gln45Lys