Canonical Allele Identifier: CA1672961482

Gene: CCDC170

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151612023G= , CM000668.2:g.151612023G=	GRCh38
NC_000006.11:g.151933158G= , CM000668.1:g.151933158G=	GRCh37
NC_000006.10:g.151974851G=	NCBI36
NG_021198.1:g.122984G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000239374.8:c.1711-3420G= MANE Select	ENSP00000239374.6:n.1711-3420G=
ENST00000239374.7:c.1711-3420G=	ENSP00000239374.6:n.1711-3420G=
ENST00000537358.1:n.497-3420G=
NM_025059.3:c.1711-3420G=	NP_079335.2:n.1711-3420G=
XM_011536147.1:c.1729-3420G=	XP_011534449.1:n.1729-3420G=
XM_011536148.1:c.1528-3420G=	XP_011534450.1:n.1528-3420G=
XM_011536147.2:c.1729-3420G=	XP_011534449.1:n.1729-3420G=
XM_011536148.2:c.1528-3420G=	XP_011534450.1:n.1528-3420G=
XR_001743865.1:n.130-751C=
NM_025059.4:c.1711-3420G= MANE Select	NP_079335.2:n.1711-3420G=