Canonical Allele Identifier: CA46641981
Gene: EPCAM HGNC NCBI

Linked Data

dbSNP Id: rs377644504
gnomAD v4: 2-47377183-AG-A
MyVariant Identifiers: chr2:g.47604323del (hg19) chr2:g.47377184del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47377184del , CM000664.2:g.47377184del GRCh38
NC_000002.11:g.47604323del , CM000664.1:g.47604323del GRCh37
NC_000002.10:g.47457827del NCBI36
NG_012352.2:g.37022del , LRG_215:g.37022del

Transcript Alleles

HGVS Amino-acid Change
ENST00000263735.9:c.555+107del MANE Select ENSP00000263735.4:n.555+107del
ENST00000263735.8:c.555+107del ENSP00000263735.4:n.555+107del
ENST00000405271.5:c.639+107del ENSP00000385476.1:n.639+107del
ENST00000456133.5:c.639+107del ENSP00000410675.1:n.639+107del
ENST00000490733.1:n.404+107del
NM_002354.2:c.555+107del , LRG_215t1:c.555+107del NP_002345.2:n.555+107del
NM_002354.3:c.555+107del MANE Select NP_002345.2:n.555+107del
Search 100 bp 5'
Search 100 bp 3'