Canonical Allele Identifier: CA150156390

Gene: CCDC170

Linked Data

• dbSNP Id: rs878918535
• gnomAD v3: 6-151618728-G-A
• gnomAD v4: 6-151618728-G-A
• MyVariant Identifiers: chr6:g.151939863G>A (hg19) ; chr6:g.151618728G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151618728G>A , CM000668.2:g.151618728G>A	GRCh38
NC_000006.11:g.151939863G>A , CM000668.1:g.151939863G>A	GRCh37
NC_000006.10:g.151981556G>A	NCBI36
NG_021198.1:g.129689G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000239374.8:c.*581G>A MANE Select	ENSP00000239374.6:n.*581G>A
ENST00000239374.7:c.*581G>A	ENSP00000239374.6:n.*581G>A
NM_025059.3:c.*581G>A	NP_079335.2:n.*581G>A
XM_011536147.1:c.*581G>A	XP_011534449.1:n.*581G>A
XM_011536148.1:c.*581G>A	XP_011534450.1:n.*581G>A
XM_011536147.2:c.*581G>A	XP_011534449.1:n.*581G>A
XM_011536148.2:c.*581G>A	XP_011534450.1:n.*581G>A
NM_025059.4:c.*581G>A MANE Select	NP_079335.2:n.*581G>A