Canonical Allele Identifier: CA366066631

Gene: CCDC170

Linked Data

• MyVariant Identifiers: chr6:g.151936587T>A (hg19) ; chr6:g.151615452T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151615452T>A , CM000668.2:g.151615452T>A	GRCh38
NC_000006.11:g.151936587T>A , CM000668.1:g.151936587T>A	GRCh37
NC_000006.10:g.151978280T>A	NCBI36
NG_021198.1:g.126413T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000239374.8:c.1720T>A MANE Select	ENSP00000239374.6:p.Leu574Met
ENST00000239374.7:c.1720T>A	ENSP00000239374.6:p.Leu574Met
ENST00000537358.1:n.506T>A
NM_025059.3:c.1720T>A	NP_079335.2:p.Leu574Met
XM_011536147.1:c.1738T>A	XP_011534449.1:p.Leu580Met
XM_011536148.1:c.1537T>A	XP_011534450.1:p.Leu513Met
XM_011536147.2:c.1738T>A	XP_011534449.1:p.Leu580Met
XM_011536148.2:c.1537T>A	XP_011534450.1:p.Leu513Met
XR_001743865.1:n.129+1269A>T
NM_025059.4:c.1720T>A MANE Select	NP_079335.2:p.Leu574Met