Canonical Allele Identifier: CA366066654

Gene: CCDC170

Linked Data

• dbSNP Id: rs1776948566
• MyVariant Identifiers: chr6:g.151936591A>G (hg19) ; chr6:g.151615456A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151615456A>G , CM000668.2:g.151615456A>G	GRCh38
NC_000006.11:g.151936591A>G , CM000668.1:g.151936591A>G	GRCh37
NC_000006.10:g.151978284A>G	NCBI36
NG_021198.1:g.126417A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000239374.8:c.1724A>G MANE Select	ENSP00000239374.6:p.Glu575Gly
ENST00000239374.7:c.1724A>G	ENSP00000239374.6:p.Glu575Gly
ENST00000537358.1:n.510A>G
NM_025059.3:c.1724A>G	NP_079335.2:p.Glu575Gly
XM_011536147.1:c.1742A>G	XP_011534449.1:p.Glu581Gly
XM_011536148.1:c.1541A>G	XP_011534450.1:p.Glu514Gly
XM_011536147.2:c.1742A>G	XP_011534449.1:p.Glu581Gly
XM_011536148.2:c.1541A>G	XP_011534450.1:p.Glu514Gly
XR_001743865.1:n.129+1265T>C
NM_025059.4:c.1724A>G MANE Select	NP_079335.2:p.Glu575Gly