Canonical Allele Identifier: CA425947365
Gene: EPCAM HGNC NCBI

Linked Data

gnomAD v4: 2-47377035-A-G
MyVariant Identifiers: chr2:g.47604174A>G (hg19)

Genomic Alleles

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

Transcript Alleles

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