Canonical Allele Identifier: CA1672964298

Gene: CCDC170

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151615446A= , CM000668.2:g.151615446A=	GRCh38
NC_000006.11:g.151936581A= , CM000668.1:g.151936581A=	GRCh37
NC_000006.10:g.151978274A=	NCBI36
NG_021198.1:g.126407A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000239374.8:c.1714A= MANE Select	ENSP00000239374.6:p.Lys572=
ENST00000239374.7:c.1714A=	ENSP00000239374.6:p.Lys572=
ENST00000537358.1:n.500A=
NM_025059.3:c.1714A=	NP_079335.2:p.Lys572=
XM_011536147.1:c.1732A=	XP_011534449.1:p.Lys578=
XM_011536148.1:c.1531A=	XP_011534450.1:p.Lys511=
XM_011536147.2:c.1732A=	XP_011534449.1:p.Lys578=
XM_011536148.2:c.1531A=	XP_011534450.1:p.Lys511=
XR_001743865.1:n.129+1275T=
NM_025059.4:c.1714A= MANE Select	NP_079335.2:p.Lys572=