Canonical Allele Identifier: CA1672965874

Gene: CCDC170

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151618130T= , CM000668.2:g.151618130T=	GRCh38
NC_000006.11:g.151939265T= , CM000668.1:g.151939265T=	GRCh37
NC_000006.10:g.151980958T=	NCBI36
NG_021198.1:g.129091T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000239374.8:c.2131T= MANE Select	ENSP00000239374.6:p.Leu711=
ENST00000239374.7:c.2131T=	ENSP00000239374.6:p.Leu711=
NM_025059.3:c.2131T=	NP_079335.2:p.Leu711=
XM_011536147.1:c.2149T=	XP_011534449.1:p.Leu717=
XM_011536148.1:c.1948T=	XP_011534450.1:p.Leu650=
XM_011536147.2:c.2149T=	XP_011534449.1:p.Leu717=
XM_011536148.2:c.1948T=	XP_011534450.1:p.Leu650=
NM_025059.4:c.2131T= MANE Select	NP_079335.2:p.Leu711=