Canonical Allele Identifier: CA150160099

Gene: CCDC170

Linked Data

• dbSNP Id: rs961537153
• gnomAD v2: 6-151901338-G-A
• gnomAD v3: 6-151580203-G-A
• gnomAD v4: 6-151580203-G-A
• MyVariant Identifiers: chr6:g.151901338G>A (hg19) ; chr6:g.151580203G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151580203G>A , CM000668.2:g.151580203G>A	GRCh38
NC_000006.11:g.151901338G>A , CM000668.1:g.151901338G>A	GRCh37
NC_000006.10:g.151943031G>A	NCBI36
NG_021198.1:g.91164G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000239374.8:c.1093-5686G>A MANE Select	ENSP00000239374.6:n.1093-5686G>A
ENST00000239374.7:c.1093-5686G>A	ENSP00000239374.6:n.1093-5686G>A
NM_025059.3:c.1093-5686G>A	NP_079335.2:n.1093-5686G>A
XM_011536147.1:c.1111-5686G>A	XP_011534449.1:n.1111-5686G>A
XM_011536148.1:c.1110+6712G>A	XP_011534450.1:n.1110+6712G>A
XM_011536147.2:c.1111-5686G>A	XP_011534449.1:n.1111-5686G>A
XM_011536148.2:c.1110+6712G>A	XP_011534450.1:n.1110+6712G>A
NM_025059.4:c.1093-5686G>A MANE Select	NP_079335.2:n.1093-5686G>A