Canonical Allele Identifier: CA346724067
Gene: EPCAM HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.47604213T>G (hg19) chr2:g.47377074T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47377074T>G , CM000664.2:g.47377074T>G GRCh38
NC_000002.11:g.47604213T>G , CM000664.1:g.47604213T>G GRCh37
NC_000002.10:g.47457717T>G NCBI36
NG_012352.2:g.36912T>G , LRG_215:g.36912T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000263735.9:c.552T>G MANE Select ENSP00000263735.4:p.Ile184Met
ENST00000263735.8:c.552T>G ENSP00000263735.4:p.Ile184Met
ENST00000405271.5:c.636T>G ENSP00000385476.1:p.Ile212Met
ENST00000456133.5:c.636T>G ENSP00000410675.1:p.Ile212Met
ENST00000490733.1:n.401T>G
NM_002354.2:c.552T>G , LRG_215t1:c.552T>G NP_002345.2:p.Ile184Met
NM_002354.3:c.552T>G MANE Select NP_002345.2:p.Ile184Met
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