Canonical Allele Identifier: CA1672962402

Gene: CCDC170

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151615510T= , CM000668.2:g.151615510T=	GRCh38
NC_000006.11:g.151936645T= , CM000668.1:g.151936645T=	GRCh37
NC_000006.10:g.151978338T=	NCBI36
NG_021198.1:g.126471T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000239374.8:c.1778T= MANE Select	ENSP00000239374.6:p.Met593=
ENST00000239374.7:c.1778T=	ENSP00000239374.6:p.Met593=
ENST00000537358.1:n.564T=
NM_025059.3:c.1778T=	NP_079335.2:p.Met593=
XM_011536147.1:c.1796T=	XP_011534449.1:p.Met599=
XM_011536148.1:c.1595T=	XP_011534450.1:p.Met532=
XM_011536147.2:c.1796T=	XP_011534449.1:p.Met599=
XM_011536148.2:c.1595T=	XP_011534450.1:p.Met532=
XR_001743865.1:n.129+1211A=
NM_025059.4:c.1778T= MANE Select	NP_079335.2:p.Met593=