Canonical Allele Identifier: CA150154158

Gene: CCDC170

Linked Data

• dbSNP Id: rs528251554
• gnomAD v3: 6-151612001-G-A
• gnomAD v4: 6-151612001-G-A
• MyVariant Identifiers: chr6:g.151933136G>A (hg19) ; chr6:g.151612001G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151612001G>A , CM000668.2:g.151612001G>A	GRCh38
NC_000006.11:g.151933136G>A , CM000668.1:g.151933136G>A	GRCh37
NC_000006.10:g.151974829G>A	NCBI36
NG_021198.1:g.122962G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000239374.8:c.1711-3442G>A MANE Select	ENSP00000239374.6:n.1711-3442G>A
ENST00000239374.7:c.1711-3442G>A	ENSP00000239374.6:n.1711-3442G>A
ENST00000537358.1:n.497-3442G>A
NM_025059.3:c.1711-3442G>A	NP_079335.2:n.1711-3442G>A
XM_011536147.1:c.1729-3442G>A	XP_011534449.1:n.1729-3442G>A
XM_011536148.1:c.1528-3442G>A	XP_011534450.1:n.1528-3442G>A
XM_011536147.2:c.1729-3442G>A	XP_011534449.1:n.1729-3442G>A
XM_011536148.2:c.1528-3442G>A	XP_011534450.1:n.1528-3442G>A
XR_001743865.1:n.130-729C>T
NM_025059.4:c.1711-3442G>A MANE Select	NP_079335.2:n.1711-3442G>A