Canonical Allele Identifier: CA1672962536

Gene: CCDC170

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151615592A= , CM000668.2:g.151615592A=	GRCh38
NC_000006.11:g.151936727A= , CM000668.1:g.151936727A=	GRCh37
NC_000006.10:g.151978420A=	NCBI36
NG_021198.1:g.126553A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000239374.8:c.1860A= MANE Select	ENSP00000239374.6:p.Glu620=
ENST00000239374.7:c.1860A=	ENSP00000239374.6:p.Glu620=
NM_025059.3:c.1860A=	NP_079335.2:p.Glu620=
XM_011536147.1:c.1878A=	XP_011534449.1:p.Glu626=
XM_011536148.1:c.1677A=	XP_011534450.1:p.Glu559=
XM_011536147.2:c.1878A=	XP_011534449.1:p.Glu626=
XM_011536148.2:c.1677A=	XP_011534450.1:p.Glu559=
XR_001743865.1:n.129+1129T=
NM_025059.4:c.1860A= MANE Select	NP_079335.2:p.Glu620=