Canonical Allele Identifier: CA1672965855

Gene: CCDC170

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151618119C= , CM000668.2:g.151618119C=	GRCh38
NC_000006.11:g.151939254C= , CM000668.1:g.151939254C=	GRCh37
NC_000006.10:g.151980947C=	NCBI36
NG_021198.1:g.129080C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000239374.8:c.2120C= MANE Select	ENSP00000239374.6:p.Pro707=
ENST00000239374.7:c.2120C=	ENSP00000239374.6:p.Pro707=
NM_025059.3:c.2120C=	NP_079335.2:p.Pro707=
XM_011536147.1:c.2138C=	XP_011534449.1:p.Pro713=
XM_011536148.1:c.1937C=	XP_011534450.1:p.Pro646=
XM_011536147.2:c.2138C=	XP_011534449.1:p.Pro713=
XM_011536148.2:c.1937C=	XP_011534450.1:p.Pro646=
NM_025059.4:c.2120C= MANE Select	NP_079335.2:p.Pro707=