Canonical Allele Identifier: CA346723962
Gene: EPCAM HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47377025A>G , CM000664.2:g.47377025A>G GRCh38
NC_000002.11:g.47604164A>G , CM000664.1:g.47604164A>G GRCh37
NC_000002.10:g.47457668A>G NCBI36
NG_012352.2:g.36863A>G , LRG_215:g.36863A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000263735.9:c.503A>G MANE Select ENSP00000263735.4:p.Lys168Arg
ENST00000263735.8:c.503A>G ENSP00000263735.4:p.Lys168Arg
ENST00000405271.5:c.587A>G ENSP00000385476.1:p.Lys196Arg
ENST00000456133.5:c.587A>G ENSP00000410675.1:p.Lys196Arg
ENST00000490733.1:n.352A>G
NM_002354.2:c.503A>G , LRG_215t1:c.503A>G NP_002345.2:p.Lys168Arg
NM_002354.3:c.503A>G MANE Select NP_002345.2:p.Lys168Arg