Canonical Allele Identifier: CA1980446356

Gene: NDUFS8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68032952G= , CM000673.2:g.68032952G=	GRCh38
NC_000011.9:g.67800419G= , CM000673.1:g.67800419G=	GRCh37
NC_000011.8:g.67556995G=	NCBI36
NG_017040.1:g.7336G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313468.10:c.139G= MANE Select	ENSP00000315774.5:p.Asp47=
ENST00000313468.9:c.139G=	ENSP00000315774.5:p.Asp47=
ENST00000432321.6:n.256G=
ENST00000453471.6:c.139G=	ENSP00000403972.2:p.Asp47=
ENST00000525419.5:c.85G=	ENSP00000433521.1:p.Asp29=
ENST00000525628.1:c.139G=	ENSP00000432968.1:p.Asp47=
ENST00000526339.5:c.139G=	ENSP00000436287.1:p.Asp47=
ENST00000526446.5:c.*194G=	ENSP00000433645.1:n.*194G=
ENST00000528492.1:c.-67+2219G=	ENSP00000432848.1:n.-67+2219G=
ENST00000529645.1:c.317G=	ENSP00000431293.1:n.317G=
ENST00000531228.1:c.194G=	ENSP00000433054.1:p.Gly65=
ENST00000532399.1:n.746G=
NM_002496.3:c.139G=	NP_002487.1:p.Asp47=
XM_005274013.1:c.139G=	XP_005274070.1:p.Asp47=
XM_005274014.1:c.139G=	XP_005274071.1:p.Asp47=
XM_005274015.1:c.19G=	XP_005274072.1:p.Asp7=
XM_011545053.1:c.139G=	XP_011543355.1:p.Asp47=
NM_002496.4:c.139G= MANE Select	NP_002487.1:p.Asp47=