Canonical Allele Identifier: CA1980447037

Gene: NDUFS8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68033210C= , CM000673.2:g.68033210C=	GRCh38
NC_000011.9:g.67800677C= , CM000673.1:g.67800677C=	GRCh37
NC_000011.8:g.67557253C=	NCBI36
NG_017040.1:g.7594C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313468.10:c.299C= MANE Select	ENSP00000315774.5:p.Ala100=
ENST00000313468.9:c.299C=	ENSP00000315774.5:p.Ala100=
ENST00000432321.6:n.416C=
ENST00000453471.6:c.299C=	ENSP00000403972.2:p.Ala100=
ENST00000524810.5:c.70C=
ENST00000525419.5:c.245C=	ENSP00000433521.1:p.Ala82=
ENST00000525628.1:c.299C=	ENSP00000432968.1:p.Ala100=
ENST00000526339.5:c.299C=	ENSP00000436287.1:p.Ala100=
ENST00000526446.5:c.*354C=	ENSP00000433645.1:n.*354C=
ENST00000528492.1:c.-67+2477C=	ENSP00000432848.1:n.-67+2477C=
ENST00000529645.1:c.477C=	ENSP00000431293.1:n.477C=
ENST00000531228.1:c.*141C=	ENSP00000433054.1:n.*141C=
ENST00000532399.1:n.1004C=
NM_002496.3:c.299C=	NP_002487.1:p.Ala100=
XM_005274013.1:c.299C=	XP_005274070.1:p.Ala100=
XM_005274014.1:c.299C=	XP_005274071.1:p.Ala100=
XM_005274015.1:c.179C=	XP_005274072.1:p.Ala60=
XM_011545053.1:c.299C=	XP_011543355.1:p.Ala100=
NM_002496.4:c.299C= MANE Select	NP_002487.1:p.Ala100=