Canonical Allele Identifier: CA2699185486
Gene: EPCAM HGNC NCBI

Linked Data

dbSNP Id: rs2103752979
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47376945del , CM000664.2:g.47376945del GRCh38
NC_000002.11:g.47604084del , CM000664.1:g.47604084del GRCh37
NC_000002.10:g.47457588del NCBI36
NG_012352.2:g.36783del , LRG_215:g.36783del

Transcript Alleles

HGVS Amino-acid Change
ENST00000263735.9:c.492-69del MANE Select ENSP00000263735.4:n.492-69del
ENST00000263735.8:c.492-69del ENSP00000263735.4:n.492-69del
ENST00000405271.5:c.576-69del ENSP00000385476.1:n.576-69del
ENST00000456133.5:c.576-69del ENSP00000410675.1:n.576-69del
ENST00000490733.1:n.341-69del
NM_002354.2:c.492-69del , LRG_215t1:c.492-69del NP_002345.2:n.492-69del
NM_002354.3:c.492-69del MANE Select NP_002345.2:n.492-69del
Search 100 bp 5'
Search 100 bp 3'