Canonical Allele Identifier: CA2495810700
Gene: EPCAM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47377229_47377230delinsGT , CM000664.2:g.47377229_47377230delinsGT GRCh38
NC_000002.11:g.47604368_47604369delinsGT , CM000664.1:g.47604368_47604369delinsGT GRCh37
NC_000002.10:g.47457872_47457873delinsGT NCBI36
NG_012352.2:g.37067_37068delinsGT , LRG_215:g.37067_37068delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000263735.9:c.555+152_555+153delinsGT MANE Select ENSP00000263735.4:n.555+152_555+153delinsGT
ENST00000263735.8:c.555+152_555+153delinsGT ENSP00000263735.4:n.555+152_555+153delinsGT
ENST00000405271.5:c.639+152_639+153delinsGT ENSP00000385476.1:n.639+152_639+153delinsGT
ENST00000456133.5:c.639+152_639+153delinsGT ENSP00000410675.1:n.639+152_639+153delinsGT
ENST00000490733.1:n.404+152_404+153delinsGT
NM_002354.2:c.555+152_555+153delinsGT , LRG_215t1:c.555+152_555+153delinsGT NP_002345.2:n.555+152_555+153delinsGT
NM_002354.3:c.555+152_555+153delinsGT MANE Select NP_002345.2:n.555+152_555+153delinsGT