Canonical Allele Identifier: CA1672964292

Gene: CCDC170

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151615442G= , CM000668.2:g.151615442G=	GRCh38
NC_000006.11:g.151936577G= , CM000668.1:g.151936577G=	GRCh37
NC_000006.10:g.151978270G=	NCBI36
NG_021198.1:g.126403G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000239374.8:c.1711-1G= MANE Select	ENSP00000239374.6:n.1711-1G=
ENST00000239374.7:c.1711-1G=	ENSP00000239374.6:n.1711-1G=
ENST00000537358.1:n.497-1G=
NM_025059.3:c.1711-1G=	NP_079335.2:n.1711-1G=
XM_011536147.1:c.1729-1G=	XP_011534449.1:n.1729-1G=
XM_011536148.1:c.1528-1G=	XP_011534450.1:n.1528-1G=
XM_011536147.2:c.1729-1G=	XP_011534449.1:n.1729-1G=
XM_011536148.2:c.1528-1G=	XP_011534450.1:n.1528-1G=
XR_001743865.1:n.129+1279C=
NM_025059.4:c.1711-1G= MANE Select	NP_079335.2:n.1711-1G=