Canonical Allele Identifier: CA3091214210

Gene: EPCAM

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47373967_47373968delinsCT , CM000664.2:g.47373967_47373968delinsCT	GRCh38
NC_000002.11:g.47601106_47601107delinsCT , CM000664.1:g.47601106_47601107delinsCT	GRCh37
NC_000002.10:g.47454610_47454611delinsCT	NCBI36
NG_012352.2:g.33805_33806delinsCT , LRG_215:g.33805_33806delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263735.9:c.344_345delinsCT MANE Select	ENSP00000263735.4:p.Met115Thr
ENST00000263735.8:c.344_345delinsCT	ENSP00000263735.4:p.Met115Thr
ENST00000405271.5:c.428_429delinsCT	ENSP00000385476.1:p.Met143Thr
ENST00000419334.1:c.572_573delinsCT	ENSP00000389028.1:p.Met191Thr
ENST00000456133.5:c.428_429delinsCT	ENSP00000410675.1:p.Met143Thr
ENST00000474691.1:n.612_613delinsCT
ENST00000490733.1:n.193_194delinsCT
NM_002354.2:c.344_345delinsCT , LRG_215t1:c.344_345delinsCT	NP_002345.2:p.Met115Thr
NM_002354.3:c.344_345delinsCT MANE Select	NP_002345.2:p.Met115Thr