Canonical Allele Identifier: CA366067841

Gene: CCDC170

Linked Data

• gnomAD v4: 6-151615608-A-G
• MyVariant Identifiers: chr6:g.151936743A>G (hg19) ; chr6:g.151615608A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151615608A>G , CM000668.2:g.151615608A>G	GRCh38
NC_000006.11:g.151936743A>G , CM000668.1:g.151936743A>G	GRCh37
NC_000006.10:g.151978436A>G	NCBI36
NG_021198.1:g.126569A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000239374.8:c.1876A>G MANE Select	ENSP00000239374.6:p.Ile626Val
ENST00000239374.7:c.1876A>G	ENSP00000239374.6:p.Ile626Val
NM_025059.3:c.1876A>G	NP_079335.2:p.Ile626Val
XM_011536147.1:c.1894A>G	XP_011534449.1:p.Ile632Val
XM_011536148.1:c.1693A>G	XP_011534450.1:p.Ile565Val
XM_011536147.2:c.1894A>G	XP_011534449.1:p.Ile632Val
XM_011536148.2:c.1693A>G	XP_011534450.1:p.Ile565Val
XR_001743865.1:n.129+1113T>C
NM_025059.4:c.1876A>G MANE Select	NP_079335.2:p.Ile626Val