Canonical Allele Identifier: CA2773569069

Gene: CCDC170

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151526930C>A , CM000668.2:g.151526930C>A	GRCh38
NC_000006.11:g.151848065C>A , CM000668.1:g.151848065C>A	GRCh37
NC_000006.10:g.151889758C>A	NCBI36
NG_021198.1:g.37891C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000239374.8:c.58-9388C>A MANE Select	ENSP00000239374.6:n.58-9388C>A
ENST00000239374.7:c.58-9388C>A	ENSP00000239374.6:n.58-9388C>A
NM_025059.3:c.58-9388C>A	NP_079335.2:n.58-9388C>A
NM_025059.4:c.58-9388C>A MANE Select	NP_079335.2:n.58-9388C>A