Canonical Allele Identifier: CA1980447250

Gene: NDUFS8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68033254A= , CM000673.2:g.68033254A=	GRCh38
NC_000011.9:g.67800721A= , CM000673.1:g.67800721A=	GRCh37
NC_000011.8:g.67557297A=	NCBI36
NG_017040.1:g.7638A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313468.10:c.343A= MANE Select	ENSP00000315774.5:p.Lys115=
ENST00000313468.9:c.343A=	ENSP00000315774.5:p.Lys115=
ENST00000432321.6:n.460A=
ENST00000453471.6:c.343A=	ENSP00000403972.2:p.Lys115=
ENST00000524810.5:c.114A=
ENST00000525419.5:c.289A=	ENSP00000433521.1:p.Lys97=
ENST00000526339.5:c.343A=	ENSP00000436287.1:p.Lys115=
ENST00000526446.5:c.*398A=	ENSP00000433645.1:n.*398A=
ENST00000528492.1:c.-67+2521A=	ENSP00000432848.1:n.-67+2521A=
ENST00000529645.1:c.521A=	ENSP00000431293.1:n.521A=
ENST00000532399.1:n.1048A=
NM_002496.3:c.343A=	NP_002487.1:p.Lys115=
XM_005274013.1:c.343A=	XP_005274070.1:p.Lys115=
XM_005274014.1:c.343A=	XP_005274071.1:p.Lys115=
XM_005274015.1:c.223A=	XP_005274072.1:p.Lys75=
XM_011545053.1:c.343A=	XP_011543355.1:p.Lys115=
NM_002496.4:c.343A= MANE Select	NP_002487.1:p.Lys115=