Canonical Allele Identifier: CA2658944349
Gene: EPCAM HGNC NCBI

Linked Data

gnomAD v4: 2-47377083-AT-A
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47377089del , CM000664.2:g.47377089del GRCh38
NC_000002.11:g.47604228del , CM000664.1:g.47604228del GRCh37
NC_000002.10:g.47457732del NCBI36
NG_012352.2:g.36927del , LRG_215:g.36927del

Transcript Alleles

HGVS Amino-acid Change
ENST00000263735.9:c.555+12del MANE Select ENSP00000263735.4:n.555+12del
ENST00000263735.8:c.555+12del ENSP00000263735.4:n.555+12del
ENST00000405271.5:c.639+12del ENSP00000385476.1:n.639+12del
ENST00000456133.5:c.639+12del ENSP00000410675.1:n.639+12del
ENST00000490733.1:n.404+12del
NM_002354.2:c.555+12del , LRG_215t1:c.555+12del NP_002345.2:n.555+12del
NM_002354.3:c.555+12del MANE Select NP_002345.2:n.555+12del
Search 100 bp 5'
Search 100 bp 3'