Canonical Allele Identifier: CA2699185529

Gene: EPCAM

Linked Data

• dbSNP Id: rs2103752988

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47376945A>T , CM000664.2:g.47376945A>T	GRCh38
NC_000002.11:g.47604084A>T , CM000664.1:g.47604084A>T	GRCh37
NC_000002.10:g.47457588A>T	NCBI36
NG_012352.2:g.36783A>T , LRG_215:g.36783A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263735.9:c.492-69A>T MANE Select	ENSP00000263735.4:n.492-69A>T
ENST00000263735.8:c.492-69A>T	ENSP00000263735.4:n.492-69A>T
ENST00000405271.5:c.576-69A>T	ENSP00000385476.1:n.576-69A>T
ENST00000456133.5:c.576-69A>T	ENSP00000410675.1:n.576-69A>T
ENST00000490733.1:n.341-69A>T
NM_002354.2:c.492-69A>T , LRG_215t1:c.492-69A>T	NP_002345.2:n.492-69A>T
NM_002354.3:c.492-69A>T MANE Select	NP_002345.2:n.492-69A>T