Canonical Allele Identifier: CA2586964804

Gene: EPCAM

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47373967_47373968delinsCC , CM000664.2:g.47373967_47373968delinsCC	GRCh38
NC_000002.11:g.47601106_47601107delinsCC , CM000664.1:g.47601106_47601107delinsCC	GRCh37
NC_000002.10:g.47454610_47454611delinsCC	NCBI36
NG_012352.2:g.33805_33806delinsCC , LRG_215:g.33805_33806delinsCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263735.9:c.344_345delinsCC MANE Select	ENSP00000263735.4:p.Met115Thr
ENST00000263735.8:c.344_345delinsCC	ENSP00000263735.4:p.Met115Thr
ENST00000405271.5:c.428_429delinsCC	ENSP00000385476.1:p.Met143Thr
ENST00000419334.1:c.572_573delinsCC	ENSP00000389028.1:p.Met191Thr
ENST00000456133.5:c.428_429delinsCC	ENSP00000410675.1:p.Met143Thr
ENST00000474691.1:n.612_613delinsCC
ENST00000490733.1:n.193_194delinsCC
NM_002354.2:c.344_345delinsCC , LRG_215t1:c.344_345delinsCC	NP_002345.2:p.Met115Thr
NM_002354.3:c.344_345delinsCC MANE Select	NP_002345.2:p.Met115Thr