Canonical Allele Identifier: CA425947363
Gene: EPCAM HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.47604174A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47377035A>C , CM000664.2:g.47377035A>C GRCh38
NC_000002.11:g.47604174A>C , CM000664.1:g.47604174A>C GRCh37
NC_000002.10:g.47457678A>C NCBI36
NG_012352.2:g.36873A>C , LRG_215:g.36873A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000263735.9:c.513A>C MANE Select ENSP00000263735.4:p.Thr171=
ENST00000263735.8:c.513A>C ENSP00000263735.4:p.Thr171=
ENST00000405271.5:c.597A>C ENSP00000385476.1:p.Thr199=
ENST00000456133.5:c.597A>C ENSP00000410675.1:p.Thr199=
ENST00000490733.1:n.362A>C
NM_002354.2:c.513A>C , LRG_215t1:c.513A>C NP_002345.2:p.Thr171=
NM_002354.3:c.513A>C MANE Select NP_002345.2:p.Thr171=