Canonical Allele Identifier: CA2495810690
Gene: EPCAM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47377196G= , CM000664.2:g.47377196G= GRCh38
NC_000002.11:g.47604335G= , CM000664.1:g.47604335G= GRCh37
NC_000002.10:g.47457839G= NCBI36
NG_012352.2:g.37034G= , LRG_215:g.37034G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263735.9:c.555+119G= MANE Select ENSP00000263735.4:n.555+119G=
ENST00000263735.8:c.555+119G= ENSP00000263735.4:n.555+119G=
ENST00000405271.5:c.639+119G= ENSP00000385476.1:n.639+119G=
ENST00000456133.5:c.639+119G= ENSP00000410675.1:n.639+119G=
ENST00000490733.1:n.404+119G=
NM_002354.2:c.555+119G= , LRG_215t1:c.555+119G= NP_002345.2:n.555+119G=
NM_002354.3:c.555+119G= MANE Select NP_002345.2:n.555+119G=