Canonical Allele Identifier: CA346723964
Gene: EPCAM HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.47604164A>C (hg19) chr2:g.47377025A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47377025A>C , CM000664.2:g.47377025A>C GRCh38
NC_000002.11:g.47604164A>C , CM000664.1:g.47604164A>C GRCh37
NC_000002.10:g.47457668A>C NCBI36
NG_012352.2:g.36863A>C , LRG_215:g.36863A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000263735.9:c.503A>C MANE Select ENSP00000263735.4:p.Lys168Thr
ENST00000263735.8:c.503A>C ENSP00000263735.4:p.Lys168Thr
ENST00000405271.5:c.587A>C ENSP00000385476.1:p.Lys196Thr
ENST00000456133.5:c.587A>C ENSP00000410675.1:p.Lys196Thr
ENST00000490733.1:n.352A>C
NM_002354.2:c.503A>C , LRG_215t1:c.503A>C NP_002345.2:p.Lys168Thr
NM_002354.3:c.503A>C MANE Select NP_002345.2:p.Lys168Thr
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