Canonical Allele Identifier: CA2749800300
Gene: EPCAM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47377199_47377200insCGAAAC , CM000664.2:g.47377199_47377200insCGAAAC GRCh38
NC_000002.11:g.47604338_47604339insCGAAAC , CM000664.1:g.47604338_47604339insCGAAAC GRCh37
NC_000002.10:g.47457842_47457843insCGAAAC NCBI36
NG_012352.2:g.37037_37038insCGAAAC , LRG_215:g.37037_37038insCGAAAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000263735.9:c.555+122_555+123insCGAAAC MANE Select ENSP00000263735.4:n.555+122_555+123insCGAAAC
ENST00000263735.8:c.555+122_555+123insCGAAAC ENSP00000263735.4:n.555+122_555+123insCGAAAC
ENST00000405271.5:c.639+122_639+123insCGAAAC ENSP00000385476.1:n.639+122_639+123insCGAAAC
ENST00000456133.5:c.639+122_639+123insCGAAAC ENSP00000410675.1:n.639+122_639+123insCGAAAC
ENST00000490733.1:n.404+122_404+123insCGAAAC
NM_002354.2:c.555+122_555+123insCGAAAC , LRG_215t1:c.555+122_555+123insCGAAAC NP_002345.2:n.555+122_555+123insCGAAAC
NM_002354.3:c.555+122_555+123insCGAAAC MANE Select NP_002345.2:n.555+122_555+123insCGAAAC