Canonical Allele Identifier: CA1980447021

Gene: NDUFS8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68033205G= , CM000673.2:g.68033205G=	GRCh38
NC_000011.9:g.67800672G= , CM000673.1:g.67800672G=	GRCh37
NC_000011.8:g.67557248G=	NCBI36
NG_017040.1:g.7589G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313468.10:c.294G= MANE Select	ENSP00000315774.5:p.Glu98=
ENST00000313468.9:c.294G=	ENSP00000315774.5:p.Glu98=
ENST00000432321.6:n.411G=
ENST00000453471.6:c.294G=	ENSP00000403972.2:p.Glu98=
ENST00000524810.5:c.65G=
ENST00000525419.5:c.240G=	ENSP00000433521.1:p.Glu80=
ENST00000525628.1:c.294G=	ENSP00000432968.1:p.Glu98=
ENST00000526339.5:c.294G=	ENSP00000436287.1:p.Glu98=
ENST00000526446.5:c.*349G=	ENSP00000433645.1:n.*349G=
ENST00000528492.1:c.-67+2472G=	ENSP00000432848.1:n.-67+2472G=
ENST00000529645.1:c.472G=	ENSP00000431293.1:n.472G=
ENST00000531228.1:c.*136G=	ENSP00000433054.1:n.*136G=
ENST00000532399.1:n.999G=
NM_002496.3:c.294G=	NP_002487.1:p.Glu98=
XM_005274013.1:c.294G=	XP_005274070.1:p.Glu98=
XM_005274014.1:c.294G=	XP_005274071.1:p.Glu98=
XM_005274015.1:c.174G=	XP_005274072.1:p.Glu58=
XM_011545053.1:c.294G=	XP_011543355.1:p.Glu98=
NM_002496.4:c.294G= MANE Select	NP_002487.1:p.Glu98=