Canonical Allele Identifier: CA2749800297
Gene: EPCAM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47377191_47377192insAACAGGAAA , CM000664.2:g.47377191_47377192insAACAGGAAA GRCh38
NC_000002.11:g.47604330_47604331insAACAGGAAA , CM000664.1:g.47604330_47604331insAACAGGAAA GRCh37
NC_000002.10:g.47457834_47457835insAACAGGAAA NCBI36
NG_012352.2:g.37029_37030insAACAGGAAA , LRG_215:g.37029_37030insAACAGGAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000263735.9:c.555+114_555+115insAACAGGAAA MANE Select ENSP00000263735.4:n.555+114_555+115insAACAGGAAA
ENST00000263735.8:c.555+114_555+115insAACAGGAAA ENSP00000263735.4:n.555+114_555+115insAACAGGAAA
ENST00000405271.5:c.639+114_639+115insAACAGGAAA ENSP00000385476.1:n.639+114_639+115insAACAGGAAA
ENST00000456133.5:c.639+114_639+115insAACAGGAAA ENSP00000410675.1:n.639+114_639+115insAACAGGAAA
ENST00000490733.1:n.404+114_404+115insAACAGGAAA
NM_002354.2:c.555+114_555+115insAACAGGAAA , LRG_215t1:c.555+114_555+115insAACAGGAAA NP_002345.2:n.555+114_555+115insAACAGGAAA
NM_002354.3:c.555+114_555+115insAACAGGAAA MANE Select NP_002345.2:n.555+114_555+115insAACAGGAAA