Canonical Allele Identifier: CA1980446849

Gene: NDUFS8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68033131T= , CM000673.2:g.68033131T=	GRCh38
NC_000011.9:g.67800598T= , CM000673.1:g.67800598T=	GRCh37
NC_000011.8:g.67557174T=	NCBI36
NG_017040.1:g.7515T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313468.10:c.220T= MANE Select	ENSP00000315774.5:p.Tyr74=
ENST00000313468.9:c.220T=	ENSP00000315774.5:p.Tyr74=
ENST00000432321.6:n.337T=
ENST00000453471.6:c.220T=	ENSP00000403972.2:p.Tyr74=
ENST00000525419.5:c.166T=	ENSP00000433521.1:p.Tyr56=
ENST00000525628.1:c.220T=	ENSP00000432968.1:p.Tyr74=
ENST00000526339.5:c.220T=	ENSP00000436287.1:p.Tyr74=
ENST00000526446.5:c.*275T=	ENSP00000433645.1:n.*275T=
ENST00000528492.1:c.-67+2398T=	ENSP00000432848.1:n.-67+2398T=
ENST00000529645.1:c.398T=	ENSP00000431293.1:n.398T=
ENST00000531228.1:c.*62T=	ENSP00000433054.1:n.*62T=
ENST00000532399.1:n.925T=
NM_002496.3:c.220T=	NP_002487.1:p.Tyr74=
XM_005274013.1:c.220T=	XP_005274070.1:p.Tyr74=
XM_005274014.1:c.220T=	XP_005274071.1:p.Tyr74=
XM_005274015.1:c.100T=	XP_005274072.1:p.Tyr34=
XM_011545053.1:c.220T=	XP_011543355.1:p.Tyr74=
NM_002496.4:c.220T= MANE Select	NP_002487.1:p.Tyr74=