Canonical Allele Identifier: CA2495810726
Gene: EPCAM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47377273_47377274delinsCT , CM000664.2:g.47377273_47377274delinsCT GRCh38
NC_000002.11:g.47604412_47604413delinsCT , CM000664.1:g.47604412_47604413delinsCT GRCh37
NC_000002.10:g.47457916_47457917delinsCT NCBI36
NG_012352.2:g.37111_37112delinsCT , LRG_215:g.37111_37112delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000263735.9:c.555+196_555+197delinsCT MANE Select ENSP00000263735.4:n.555+196_555+197delinsCT
ENST00000263735.8:c.555+196_555+197delinsCT ENSP00000263735.4:n.555+196_555+197delinsCT
ENST00000405271.5:c.639+196_639+197delinsCT ENSP00000385476.1:n.639+196_639+197delinsCT
ENST00000456133.5:c.639+196_639+197delinsCT ENSP00000410675.1:n.639+196_639+197delinsCT
ENST00000490733.1:n.404+196_404+197delinsCT
NM_002354.2:c.555+196_555+197delinsCT , LRG_215t1:c.555+196_555+197delinsCT NP_002345.2:n.555+196_555+197delinsCT
NM_002354.3:c.555+196_555+197delinsCT MANE Select NP_002345.2:n.555+196_555+197delinsCT