Canonical Allele Identifier: CA820826793

Gene: CCDC170

Linked Data

• dbSNP Id: rs762662269
• gnomAD v3: 6-151612000-C-A
• gnomAD v4: 6-151612000-C-A
• MyVariant Identifiers: chr6:g.151933135C>A (hg19) ; chr6:g.151612000C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151612000C>A , CM000668.2:g.151612000C>A	GRCh38
NC_000006.11:g.151933135C>A , CM000668.1:g.151933135C>A	GRCh37
NC_000006.10:g.151974828C>A	NCBI36
NG_021198.1:g.122961C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000239374.8:c.1711-3443C>A MANE Select	ENSP00000239374.6:n.1711-3443C>A
ENST00000239374.7:c.1711-3443C>A	ENSP00000239374.6:n.1711-3443C>A
ENST00000537358.1:n.497-3443C>A
NM_025059.3:c.1711-3443C>A	NP_079335.2:n.1711-3443C>A
XM_011536147.1:c.1729-3443C>A	XP_011534449.1:n.1729-3443C>A
XM_011536148.1:c.1528-3443C>A	XP_011534450.1:n.1528-3443C>A
XM_011536147.2:c.1729-3443C>A	XP_011534449.1:n.1729-3443C>A
XM_011536148.2:c.1528-3443C>A	XP_011534450.1:n.1528-3443C>A
XR_001743865.1:n.130-728G>T
NM_025059.4:c.1711-3443C>A MANE Select	NP_079335.2:n.1711-3443C>A