Canonical Allele Identifier: CA346724005

Gene: EPCAM

Linked Data

• dbSNP Id: rs1476960682
• MyVariant Identifiers: chr2:g.47604185A>G (hg19) ; chr2:g.47377046A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47377046A>G , CM000664.2:g.47377046A>G	GRCh38
NC_000002.11:g.47604185A>G , CM000664.1:g.47604185A>G	GRCh37
NC_000002.10:g.47457689A>G	NCBI36
NG_012352.2:g.36884A>G , LRG_215:g.36884A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263735.9:c.524A>G MANE Select	ENSP00000263735.4:p.Gln175Arg
ENST00000263735.8:c.524A>G	ENSP00000263735.4:p.Gln175Arg
ENST00000405271.5:c.608A>G	ENSP00000385476.1:p.Gln203Arg
ENST00000456133.5:c.608A>G	ENSP00000410675.1:p.Gln203Arg
ENST00000490733.1:n.373A>G
NM_002354.2:c.524A>G , LRG_215t1:c.524A>G	NP_002345.2:p.Gln175Arg
NM_002354.3:c.524A>G MANE Select	NP_002345.2:p.Gln175Arg