Canonical Allele Identifier: CA346723967
Gene: EPCAM HGNC NCBI

Linked Data

dbSNP Id: rs2103753310
MyVariant Identifiers: chr2:g.47604166G>A (hg19) chr2:g.47377027G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47377027G>A , CM000664.2:g.47377027G>A GRCh38
NC_000002.11:g.47604166G>A , CM000664.1:g.47604166G>A GRCh37
NC_000002.10:g.47457670G>A NCBI36
NG_012352.2:g.36865G>A , LRG_215:g.36865G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000263735.9:c.505G>A MANE Select ENSP00000263735.4:p.Glu169Lys
ENST00000263735.8:c.505G>A ENSP00000263735.4:p.Glu169Lys
ENST00000405271.5:c.589G>A ENSP00000385476.1:p.Glu197Lys
ENST00000456133.5:c.589G>A ENSP00000410675.1:p.Glu197Lys
ENST00000490733.1:n.354G>A
NM_002354.2:c.505G>A , LRG_215t1:c.505G>A NP_002345.2:p.Glu169Lys
NM_002354.3:c.505G>A MANE Select NP_002345.2:p.Glu169Lys
Search 100 bp 5'
Search 100 bp 3'