Canonical Allele Identifier: CA571437261

Gene: CCDC170

Linked Data

• dbSNP Id: rs1307600689
• gnomAD v2: 6-151936771-C-CA
• gnomAD v4: 6-151615636-C-CA
• MyVariant Identifiers: chr6:g.151936771_151936772insA (hg19) ; chr6:g.151615636_151615637insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151615637dup , CM000668.2:g.151615637dup	GRCh38
NC_000006.11:g.151936772dup , CM000668.1:g.151936772dup	GRCh37
NC_000006.10:g.151978465dup	NCBI36
NG_021198.1:g.126598dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000239374.8:c.1905dup MANE Select	ENSP00000239374.6:p.Leu636ThrfsTer?
ENST00000239374.7:c.1905dup	ENSP00000239374.6:p.Leu636ThrfsTer?
NM_025059.3:c.1905dup	NP_079335.2:p.Leu636ThrfsTer?
XM_011536147.1:c.1923dup	XP_011534449.1:p.Leu642ThrfsTer?
XM_011536148.1:c.1722dup	XP_011534450.1:p.Leu575ThrfsTer?
XM_011536147.2:c.1923dup	XP_011534449.1:p.Leu642ThrfsTer?
XM_011536148.2:c.1722dup	XP_011534450.1:p.Leu575ThrfsTer?
XR_001743865.1:n.129+1084dup
NM_025059.4:c.1905dup MANE Select	NP_079335.2:p.Leu636ThrfsTer?