Canonical Allele Identifier: CA2658944281
Gene: EPCAM HGNC NCBI

Linked Data

gnomAD v4: 2-47376927-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47376927C>T , CM000664.2:g.47376927C>T GRCh38
NC_000002.11:g.47604066C>T , CM000664.1:g.47604066C>T GRCh37
NC_000002.10:g.47457570C>T NCBI36
NG_012352.2:g.36765C>T , LRG_215:g.36765C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000263735.9:c.492-87C>T MANE Select ENSP00000263735.4:n.492-87C>T
ENST00000263735.8:c.492-87C>T ENSP00000263735.4:n.492-87C>T
ENST00000405271.5:c.576-87C>T ENSP00000385476.1:n.576-87C>T
ENST00000456133.5:c.576-87C>T ENSP00000410675.1:n.576-87C>T
ENST00000490733.1:n.341-87C>T
NM_002354.2:c.492-87C>T , LRG_215t1:c.492-87C>T NP_002345.2:n.492-87C>T
NM_002354.3:c.492-87C>T MANE Select NP_002345.2:n.492-87C>T
Search 100 bp 5'
Search 100 bp 3'