Canonical Allele Identifier: CA2658944325
Gene: EPCAM HGNC NCBI

Linked Data

gnomAD v4: 2-47376980-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47376980T>A , CM000664.2:g.47376980T>A GRCh38
NC_000002.11:g.47604119T>A , CM000664.1:g.47604119T>A GRCh37
NC_000002.10:g.47457623T>A NCBI36
NG_012352.2:g.36818T>A , LRG_215:g.36818T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000263735.9:c.492-34T>A MANE Select ENSP00000263735.4:n.492-34T>A
ENST00000263735.8:c.492-34T>A ENSP00000263735.4:n.492-34T>A
ENST00000405271.5:c.576-34T>A ENSP00000385476.1:n.576-34T>A
ENST00000456133.5:c.576-34T>A ENSP00000410675.1:n.576-34T>A
ENST00000490733.1:n.341-34T>A
NM_002354.2:c.492-34T>A , LRG_215t1:c.492-34T>A NP_002345.2:n.492-34T>A
NM_002354.3:c.492-34T>A MANE Select NP_002345.2:n.492-34T>A
Search 100 bp 5'
Search 100 bp 3'