Canonical Allele Identifier: CA2495810642
Gene: EPCAM HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47377111A= , CM000664.2:g.47377111A= GRCh38
NC_000002.11:g.47604250A= , CM000664.1:g.47604250A= GRCh37
NC_000002.10:g.47457754A= NCBI36
NG_012352.2:g.36949A= , LRG_215:g.36949A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263735.9:c.555+34A= MANE Select ENSP00000263735.4:n.555+34A=
ENST00000263735.8:c.555+34A= ENSP00000263735.4:n.555+34A=
ENST00000405271.5:c.639+34A= ENSP00000385476.1:n.639+34A=
ENST00000456133.5:c.639+34A= ENSP00000410675.1:n.639+34A=
ENST00000490733.1:n.404+34A=
NM_002354.2:c.555+34A= , LRG_215t1:c.555+34A= NP_002345.2:n.555+34A=
NM_002354.3:c.555+34A= MANE Select NP_002345.2:n.555+34A=
Search 100 bp 5'
Search 100 bp 3'