Canonical Allele Identifier: CA2658944275
Gene: EPCAM HGNC NCBI

Linked Data

gnomAD v4: 2-47376916-CAGTTTT-C
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47376919_47376924del , CM000664.2:g.47376919_47376924del GRCh38
NC_000002.11:g.47604058_47604063del , CM000664.1:g.47604058_47604063del GRCh37
NC_000002.10:g.47457562_47457567del NCBI36
NG_012352.2:g.36757_36762del , LRG_215:g.36757_36762del

Transcript Alleles

HGVS Amino-acid Change
ENST00000263735.9:c.492-95_492-90del MANE Select ENSP00000263735.4:n.492-95_492-90del
ENST00000263735.8:c.492-95_492-90del ENSP00000263735.4:n.492-95_492-90del
ENST00000405271.5:c.576-95_576-90del ENSP00000385476.1:n.576-95_576-90del
ENST00000456133.5:c.576-95_576-90del ENSP00000410675.1:n.576-95_576-90del
ENST00000490733.1:n.341-95_341-90del
NM_002354.2:c.492-95_492-90del , LRG_215t1:c.492-95_492-90del NP_002345.2:n.492-95_492-90del
NM_002354.3:c.492-95_492-90del MANE Select NP_002345.2:n.492-95_492-90del
Search 100 bp 5'
Search 100 bp 3'