Canonical Allele Identifier: CA2699189862
Gene: EPCAM HGNC NCBI

Linked Data

dbSNP Id: rs2103753901
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47377239del , CM000664.2:g.47377239del GRCh38
NC_000002.11:g.47604378del , CM000664.1:g.47604378del GRCh37
NC_000002.10:g.47457882del NCBI36
NG_012352.2:g.37077del , LRG_215:g.37077del

Transcript Alleles

HGVS Amino-acid Change
ENST00000263735.9:c.555+162del MANE Select ENSP00000263735.4:n.555+162del
ENST00000263735.8:c.555+162del ENSP00000263735.4:n.555+162del
ENST00000405271.5:c.639+162del ENSP00000385476.1:n.639+162del
ENST00000456133.5:c.639+162del ENSP00000410675.1:n.639+162del
ENST00000490733.1:n.404+162del
NM_002354.2:c.555+162del , LRG_215t1:c.555+162del NP_002345.2:n.555+162del
NM_002354.3:c.555+162del MANE Select NP_002345.2:n.555+162del
Search 100 bp 5'
Search 100 bp 3'