Canonical Allele Identifier: CA1672966023

Gene: CCDC170

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151618250A= , CM000668.2:g.151618250A=	GRCh38
NC_000006.11:g.151939385A= , CM000668.1:g.151939385A=	GRCh37
NC_000006.10:g.151981078A=	NCBI36
NG_021198.1:g.129211A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000239374.8:c.*103A= MANE Select	ENSP00000239374.6:n.*103A=
ENST00000239374.7:c.*103A=	ENSP00000239374.6:n.*103A=
NM_025059.3:c.*103A=	NP_079335.2:n.*103A=
XM_011536147.1:c.*103A=	XP_011534449.1:n.*103A=
XM_011536148.1:c.*103A=	XP_011534450.1:n.*103A=
XM_011536147.2:c.*103A=	XP_011534449.1:n.*103A=
XM_011536148.2:c.*103A=	XP_011534450.1:n.*103A=
NM_025059.4:c.*103A= MANE Select	NP_079335.2:n.*103A=