Canonical Allele Identifier: CA2495810706
Gene: EPCAM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47377235_47377239delinsTTTTG , CM000664.2:g.47377235_47377239delinsTTTTG GRCh38
NC_000002.11:g.47604374_47604378delinsTTTTG , CM000664.1:g.47604374_47604378delinsTTTTG GRCh37
NC_000002.10:g.47457878_47457882delinsTTTTG NCBI36
NG_012352.2:g.37073_37077delinsTTTTG , LRG_215:g.37073_37077delinsTTTTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000263735.9:c.555+158_555+162delinsTTTTG MANE Select ENSP00000263735.4:n.555+158_555+162delinsTTTTG
ENST00000263735.8:c.555+158_555+162delinsTTTTG ENSP00000263735.4:n.555+158_555+162delinsTTTTG
ENST00000405271.5:c.639+158_639+162delinsTTTTG ENSP00000385476.1:n.639+158_639+162delinsTTTTG
ENST00000456133.5:c.639+158_639+162delinsTTTTG ENSP00000410675.1:n.639+158_639+162delinsTTTTG
ENST00000490733.1:n.404+158_404+162delinsTTTTG
NM_002354.2:c.555+158_555+162delinsTTTTG , LRG_215t1:c.555+158_555+162delinsTTTTG NP_002345.2:n.555+158_555+162delinsTTTTG
NM_002354.3:c.555+158_555+162delinsTTTTG MANE Select NP_002345.2:n.555+158_555+162delinsTTTTG