Canonical Allele Identifier: CA1980447263

Gene: NDUFS8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68033259C= , CM000673.2:g.68033259C=	GRCh38
NC_000011.9:g.67800726C= , CM000673.1:g.67800726C=	GRCh37
NC_000011.8:g.67557302C=	NCBI36
NG_017040.1:g.7643C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313468.10:c.348C= MANE Select	ENSP00000315774.5:p.Leu116=
ENST00000313468.9:c.348C=	ENSP00000315774.5:p.Leu116=
ENST00000432321.6:n.465C=
ENST00000453471.6:c.348C=	ENSP00000403972.2:p.Leu116=
ENST00000524810.5:c.119C=
ENST00000525419.5:c.294C=	ENSP00000433521.1:p.Leu98=
ENST00000526339.5:c.348C=	ENSP00000436287.1:p.Leu116=
ENST00000526446.5:c.*403C=	ENSP00000433645.1:n.*403C=
ENST00000528492.1:c.-67+2526C=	ENSP00000432848.1:n.-67+2526C=
ENST00000529645.1:c.526C=	ENSP00000431293.1:n.526C=
ENST00000532399.1:n.1053C=
NM_002496.3:c.348C=	NP_002487.1:p.Leu116=
XM_005274013.1:c.348C=	XP_005274070.1:p.Leu116=
XM_005274014.1:c.348C=	XP_005274071.1:p.Leu116=
XM_005274015.1:c.228C=	XP_005274072.1:p.Leu76=
XM_011545053.1:c.348C=	XP_011543355.1:p.Leu116=
NM_002496.4:c.348C= MANE Select	NP_002487.1:p.Leu116=