Canonical Allele Identifier: CA820828516

Gene: CCDC170

Linked Data

• dbSNP Id: rs1400866353
• gnomAD v3: 6-151615366-AC-A
• gnomAD v4: 6-151615366-AC-A
• MyVariant Identifiers: chr6:g.151936502del (hg19) ; chr6:g.151615367del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151615367del , CM000668.2:g.151615367del	GRCh38
NC_000006.11:g.151936502del , CM000668.1:g.151936502del	GRCh37
NC_000006.10:g.151978195del	NCBI36
NG_021198.1:g.126328del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000239374.8:c.1711-76del MANE Select	ENSP00000239374.6:n.1711-76del
ENST00000239374.7:c.1711-76del	ENSP00000239374.6:n.1711-76del
ENST00000537358.1:n.497-76del
NM_025059.3:c.1711-76del	NP_079335.2:n.1711-76del
XM_011536147.1:c.1729-76del	XP_011534449.1:n.1729-76del
XM_011536148.1:c.1528-76del	XP_011534450.1:n.1528-76del
XM_011536147.2:c.1729-76del	XP_011534449.1:n.1729-76del
XM_011536148.2:c.1528-76del	XP_011534450.1:n.1528-76del
XR_001743865.1:n.129+1354del
NM_025059.4:c.1711-76del MANE Select	NP_079335.2:n.1711-76del