Canonical Allele Identifier: CA425947462
Gene: EPCAM HGNC NCBI

Linked Data

COSMIC: COSM1021238
MyVariant Identifiers: chr2:g.47604213T>A (hg19)
JSON-LD

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000263735.9:c.552T>A MANE Select ENSP00000263735.4:p.Ile184=
ENST00000263735.8:c.552T>A ENSP00000263735.4:p.Ile184=
ENST00000405271.5:c.636T>A ENSP00000385476.1:p.Ile212=
ENST00000456133.5:c.636T>A ENSP00000410675.1:p.Ile212=
ENST00000490733.1:n.401T>A
NM_002354.2:c.552T>A , LRG_215t1:c.552T>A NP_002345.2:p.Ile184=
NM_002354.3:c.552T>A MANE Select NP_002345.2:p.Ile184=
Search 100 bp 5'
Search 100 bp 3'