Canonical Allele Identifier: CA346723985
Gene: EPCAM HGNC NCBI

Linked Data

dbSNP Id: rs2103753345

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47377034C>G , CM000664.2:g.47377034C>G GRCh38
NC_000002.11:g.47604173C>G , CM000664.1:g.47604173C>G GRCh37
NC_000002.10:g.47457677C>G NCBI36
NG_012352.2:g.36872C>G , LRG_215:g.36872C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000263735.9:c.512C>G MANE Select ENSP00000263735.4:p.Thr171Arg
ENST00000263735.8:c.512C>G ENSP00000263735.4:p.Thr171Arg
ENST00000405271.5:c.596C>G ENSP00000385476.1:p.Thr199Arg
ENST00000456133.5:c.596C>G ENSP00000410675.1:p.Thr199Arg
ENST00000490733.1:n.361C>G
NM_002354.2:c.512C>G , LRG_215t1:c.512C>G NP_002345.2:p.Thr171Arg
NM_002354.3:c.512C>G MANE Select NP_002345.2:p.Thr171Arg