Canonical Allele Identifier: CA2495810553
Gene: EPCAM HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47376937C= , CM000664.2:g.47376937C= GRCh38
NC_000002.11:g.47604076C= , CM000664.1:g.47604076C= GRCh37
NC_000002.10:g.47457580C= NCBI36
NG_012352.2:g.36775C= , LRG_215:g.36775C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263735.9:c.492-77C= MANE Select ENSP00000263735.4:n.492-77C=
ENST00000263735.8:c.492-77C= ENSP00000263735.4:n.492-77C=
ENST00000405271.5:c.576-77C= ENSP00000385476.1:n.576-77C=
ENST00000456133.5:c.576-77C= ENSP00000410675.1:n.576-77C=
ENST00000490733.1:n.341-77C=
NM_002354.2:c.492-77C= , LRG_215t1:c.492-77C= NP_002345.2:n.492-77C=
NM_002354.3:c.492-77C= MANE Select NP_002345.2:n.492-77C=
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