Canonical Allele Identifier: CA2495810603
Gene: EPCAM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47377029_47377032delinsGATC , CM000664.2:g.47377029_47377032delinsGATC GRCh38
NC_000002.11:g.47604168_47604171delinsGATC , CM000664.1:g.47604168_47604171delinsGATC GRCh37
NC_000002.10:g.47457672_47457675delinsGATC NCBI36
NG_012352.2:g.36867_36870delinsGATC , LRG_215:g.36867_36870delinsGATC

Transcript Alleles

HGVS Amino-acid change
ENST00000263735.9:c.507_510delinsGATC MANE Select ENSP00000263735.4:p.Glu169=
ENST00000263735.8:c.507_510delinsGATC ENSP00000263735.4:p.Glu169=
ENST00000405271.5:c.591_594delinsGATC ENSP00000385476.1:p.Glu197=
ENST00000456133.5:c.591_594delinsGATC ENSP00000410675.1:p.Glu197=
ENST00000490733.1:n.356_359delinsGATC
NM_002354.2:c.507_510delinsGATC , LRG_215t1:c.507_510delinsGATC NP_002345.2:p.Glu169=
NM_002354.3:c.507_510delinsGATC MANE Select NP_002345.2:p.Glu169=