Canonical Allele Identifier: CA2658944294
Gene: EPCAM HGNC NCBI

Linked Data

gnomAD v4: 2-47376940-C-CT
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47376942dup , CM000664.2:g.47376942dup GRCh38
NC_000002.11:g.47604081dup , CM000664.1:g.47604081dup GRCh37
NC_000002.10:g.47457585dup NCBI36
NG_012352.2:g.36780dup , LRG_215:g.36780dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000263735.9:c.492-72dup MANE Select ENSP00000263735.4:n.492-72dup
ENST00000263735.8:c.492-72dup ENSP00000263735.4:n.492-72dup
ENST00000405271.5:c.576-72dup ENSP00000385476.1:n.576-72dup
ENST00000456133.5:c.576-72dup ENSP00000410675.1:n.576-72dup
ENST00000490733.1:n.341-72dup
NM_002354.2:c.492-72dup , LRG_215t1:c.492-72dup NP_002345.2:n.492-72dup
NM_002354.3:c.492-72dup MANE Select NP_002345.2:n.492-72dup
Search 100 bp 5'
Search 100 bp 3'