Canonical Allele Identifier: CA2658944292
Gene: EPCAM HGNC NCBI

Linked Data

gnomAD v4: 2-47376939-G-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47376939G>T , CM000664.2:g.47376939G>T GRCh38
NC_000002.11:g.47604078G>T , CM000664.1:g.47604078G>T GRCh37
NC_000002.10:g.47457582G>T NCBI36
NG_012352.2:g.36777G>T , LRG_215:g.36777G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000263735.9:c.492-75G>T MANE Select ENSP00000263735.4:n.492-75G>T
ENST00000263735.8:c.492-75G>T ENSP00000263735.4:n.492-75G>T
ENST00000405271.5:c.576-75G>T ENSP00000385476.1:n.576-75G>T
ENST00000456133.5:c.576-75G>T ENSP00000410675.1:n.576-75G>T
ENST00000490733.1:n.341-75G>T
NM_002354.2:c.492-75G>T , LRG_215t1:c.492-75G>T NP_002345.2:n.492-75G>T
NM_002354.3:c.492-75G>T MANE Select NP_002345.2:n.492-75G>T
Search 100 bp 5'
Search 100 bp 3'