Canonical Allele Identifier: CA425947353
Gene: EPCAM HGNC NCBI

Linked Data

ClinVar Variation Id: 1745020
ClinVar RCV Id: RCV002351427
dbSNP Id: rs1228978298
gnomAD v2: 2-47604165-G-A
gnomAD v4: 2-47377026-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47377026G>A , CM000664.2:g.47377026G>A GRCh38
NC_000002.11:g.47604165G>A , CM000664.1:g.47604165G>A GRCh37
NC_000002.10:g.47457669G>A NCBI36
NG_012352.2:g.36864G>A , LRG_215:g.36864G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000263735.9:c.504G>A MANE Select ENSP00000263735.4:p.Lys168=
ENST00000263735.8:c.504G>A ENSP00000263735.4:p.Lys168=
ENST00000405271.5:c.588G>A ENSP00000385476.1:p.Lys196=
ENST00000456133.5:c.588G>A ENSP00000410675.1:p.Lys196=
ENST00000490733.1:n.353G>A
NM_002354.2:c.504G>A , LRG_215t1:c.504G>A NP_002345.2:p.Lys168=
NM_002354.3:c.504G>A MANE Select NP_002345.2:p.Lys168=