Canonical Allele Identifier: CA2495810733
Gene: EPCAM HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47377279C= , CM000664.2:g.47377279C= GRCh38
NC_000002.11:g.47604418C= , CM000664.1:g.47604418C= GRCh37
NC_000002.10:g.47457922C= NCBI36
NG_012352.2:g.37117C= , LRG_215:g.37117C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263735.9:c.555+202C= MANE Select ENSP00000263735.4:n.555+202C=
ENST00000263735.8:c.555+202C= ENSP00000263735.4:n.555+202C=
ENST00000405271.5:c.639+202C= ENSP00000385476.1:n.639+202C=
ENST00000456133.5:c.639+202C= ENSP00000410675.1:n.639+202C=
ENST00000490733.1:n.404+202C=
NM_002354.2:c.555+202C= , LRG_215t1:c.555+202C= NP_002345.2:n.555+202C=
NM_002354.3:c.555+202C= MANE Select NP_002345.2:n.555+202C=
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