Canonical Allele Identifier: CA1980446367

Gene: NDUFS8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68032956T= , CM000673.2:g.68032956T=	GRCh38
NC_000011.9:g.67800423T= , CM000673.1:g.67800423T=	GRCh37
NC_000011.8:g.67556999T=	NCBI36
NG_017040.1:g.7340T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313468.10:c.143T= MANE Select	ENSP00000315774.5:p.Met48=
ENST00000313468.9:c.143T=	ENSP00000315774.5:p.Met48=
ENST00000432321.6:n.260T=
ENST00000453471.6:c.143T=	ENSP00000403972.2:p.Met48=
ENST00000525419.5:c.89T=	ENSP00000433521.1:p.Met30=
ENST00000525628.1:c.143T=	ENSP00000432968.1:p.Met48=
ENST00000526339.5:c.143T=	ENSP00000436287.1:p.Met48=
ENST00000526446.5:c.*198T=	ENSP00000433645.1:n.*198T=
ENST00000528492.1:c.-67+2223T=	ENSP00000432848.1:n.-67+2223T=
ENST00000529645.1:c.321T=	ENSP00000431293.1:n.321T=
ENST00000531228.1:c.198T=	ENSP00000433054.1:p.His66=
ENST00000532399.1:n.750T=
NM_002496.3:c.143T=	NP_002487.1:p.Met48=
XM_005274013.1:c.143T=	XP_005274070.1:p.Met48=
XM_005274014.1:c.143T=	XP_005274071.1:p.Met48=
XM_005274015.1:c.23T=	XP_005274072.1:p.Met8=
XM_011545053.1:c.143T=	XP_011543355.1:p.Met48=
NM_002496.4:c.143T= MANE Select	NP_002487.1:p.Met48=