Canonical Allele Identifier: CA1672962553

Gene: CCDC170

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151615602A= , CM000668.2:g.151615602A=	GRCh38
NC_000006.11:g.151936737A= , CM000668.1:g.151936737A=	GRCh37
NC_000006.10:g.151978430A=	NCBI36
NG_021198.1:g.126563A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000239374.8:c.1870A= MANE Select	ENSP00000239374.6:p.Asn624=
ENST00000239374.7:c.1870A=	ENSP00000239374.6:p.Asn624=
NM_025059.3:c.1870A=	NP_079335.2:p.Asn624=
XM_011536147.1:c.1888A=	XP_011534449.1:p.Asn630=
XM_011536148.1:c.1687A=	XP_011534450.1:p.Asn563=
XM_011536147.2:c.1888A=	XP_011534449.1:p.Asn630=
XM_011536148.2:c.1687A=	XP_011534450.1:p.Asn563=
XR_001743865.1:n.129+1119T=
NM_025059.4:c.1870A= MANE Select	NP_079335.2:p.Asn624=