Canonical Allele Identifier: CA2576960546
Gene: EPCAM HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47377024_47377026del , CM000664.2:g.47377024_47377026del GRCh38
NC_000002.11:g.47604163_47604165del , CM000664.1:g.47604163_47604165del GRCh37
NC_000002.10:g.47457667_47457669del NCBI36
NG_012352.2:g.36862_36864del , LRG_215:g.36862_36864del

Transcript Alleles

HGVS Amino-acid Change
ENST00000263735.9:c.502_504del MANE Select ENSP00000263735.4:p.Lys168del
ENST00000263735.8:c.502_504del ENSP00000263735.4:p.Lys168del
ENST00000405271.5:c.586_588del ENSP00000385476.1:p.Lys196del
ENST00000456133.5:c.586_588del ENSP00000410675.1:p.Lys196del
ENST00000490733.1:n.351_353del
NM_002354.2:c.502_504del , LRG_215t1:c.502_504del NP_002345.2:p.Lys168del
NM_002354.3:c.502_504del MANE Select NP_002345.2:p.Lys168del