Canonical Allele Identifier: CA46693650

Gene: EPCAM

Linked Data

• dbSNP Id: rs373597944
• MyVariant Identifiers: chr2:g.47602372G>T (hg19) ; chr2:g.47375233G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47375233G>T , CM000664.2:g.47375233G>T	GRCh38
NC_000002.11:g.47602372G>T , CM000664.1:g.47602372G>T	GRCh37
NC_000002.10:g.47455876G>T	NCBI36
NG_012352.2:g.35071G>T , LRG_215:g.35071G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000263735.9:c.426-1G>T MANE Select	ENSP00000263735.4:n.426-1G>T
ENST00000263735.8:c.426-1G>T	ENSP00000263735.4:n.426-1G>T
ENST00000405271.5:c.510-1G>T	ENSP00000385476.1:n.510-1G>T
ENST00000456133.5:c.510-1G>T	ENSP00000410675.1:n.510-1G>T
ENST00000474691.1:n.694-1G>T
ENST00000490733.1:n.275-1G>T
NM_002354.2:c.426-1G>T , LRG_215t1:c.426-1G>T	NP_002345.2:n.426-1G>T
NM_002354.3:c.426-1G>T MANE Select	NP_002345.2:n.426-1G>T