Canonical Allele Identifier: CA475514053

Gene: NDUFS8

Linked Data

• MyVariant Identifiers: chr11:g.67800466T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68032999T>A , CM000673.2:g.68032999T>A	GRCh38
NC_000011.9:g.67800466T>A , CM000673.1:g.67800466T>A	GRCh37
NC_000011.8:g.67557042T>A	NCBI36
NG_017040.1:g.7383T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313468.10:c.186T>A MANE Select	ENSP00000315774.5:p.Thr62=
ENST00000313468.9:c.186T>A	ENSP00000315774.5:p.Thr62=
ENST00000432321.6:n.303T>A
ENST00000453471.6:c.186T>A	ENSP00000403972.2:p.Thr62=
ENST00000525419.5:c.132T>A	ENSP00000433521.1:p.Thr44=
ENST00000525628.1:c.186T>A	ENSP00000432968.1:p.Thr62=
ENST00000526339.5:c.186T>A	ENSP00000436287.1:p.Thr62=
ENST00000526446.5:c.*241T>A	ENSP00000433645.1:n.*241T>A
ENST00000528492.1:c.-67+2266T>A	ENSP00000432848.1:n.-67+2266T>A
ENST00000529645.1:c.364T>A	ENSP00000431293.1:n.364T>A
ENST00000531228.1:c.*28T>A	ENSP00000433054.1:n.*28T>A
ENST00000532399.1:n.793T>A
NM_002496.3:c.186T>A	NP_002487.1:p.Thr62=
XM_005274013.1:c.186T>A	XP_005274070.1:p.Thr62=
XM_005274014.1:c.186T>A	XP_005274071.1:p.Thr62=
XM_005274015.1:c.66T>A	XP_005274072.1:p.Thr22=
XM_011545053.1:c.186T>A	XP_011543355.1:p.Thr62=
NM_002496.4:c.186T>A MANE Select	NP_002487.1:p.Thr62=