Canonical Allele Identifier: CA2576960534
Gene: EPCAM HGNC NCBI

Linked Data

gnomAD v4: 2-47376935-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47376935G>T , CM000664.2:g.47376935G>T GRCh38
NC_000002.11:g.47604074G>T , CM000664.1:g.47604074G>T GRCh37
NC_000002.10:g.47457578G>T NCBI36
NG_012352.2:g.36773G>T , LRG_215:g.36773G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000263735.9:c.492-79G>T MANE Select ENSP00000263735.4:n.492-79G>T
ENST00000263735.8:c.492-79G>T ENSP00000263735.4:n.492-79G>T
ENST00000405271.5:c.576-79G>T ENSP00000385476.1:n.576-79G>T
ENST00000456133.5:c.576-79G>T ENSP00000410675.1:n.576-79G>T
ENST00000490733.1:n.341-79G>T
NM_002354.2:c.492-79G>T , LRG_215t1:c.492-79G>T NP_002345.2:n.492-79G>T
NM_002354.3:c.492-79G>T MANE Select NP_002345.2:n.492-79G>T
Search 100 bp 5'
Search 100 bp 3'