Canonical Allele Identifier: CA381599882

Gene: NDUFS8

Linked Data

• dbSNP Id: rs1854806433
• gnomAD v3: 11-68033195-T-A
• gnomAD v4: 11-68033195-T-A
• MyVariant Identifiers: chr11:g.67800662T>A (hg19) ; chr11:g.68033195T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68033195T>A , CM000673.2:g.68033195T>A	GRCh38
NC_000011.9:g.67800662T>A , CM000673.1:g.67800662T>A	GRCh37
NC_000011.8:g.67557238T>A	NCBI36
NG_017040.1:g.7579T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313468.10:c.284T>A MANE Select	ENSP00000315774.5:p.Phe95Tyr
ENST00000313468.9:c.284T>A	ENSP00000315774.5:p.Phe95Tyr
ENST00000432321.6:n.401T>A
ENST00000453471.6:c.284T>A	ENSP00000403972.2:p.Phe95Tyr
ENST00000524810.5:c.55T>A
ENST00000525419.5:c.230T>A	ENSP00000433521.1:p.Phe77Tyr
ENST00000525628.1:c.284T>A	ENSP00000432968.1:p.Phe95Tyr
ENST00000526339.5:c.284T>A	ENSP00000436287.1:p.Phe95Tyr
ENST00000526446.5:c.*339T>A	ENSP00000433645.1:n.*339T>A
ENST00000528492.1:c.-67+2462T>A	ENSP00000432848.1:n.-67+2462T>A
ENST00000529645.1:c.462T>A	ENSP00000431293.1:n.462T>A
ENST00000531228.1:c.*126T>A	ENSP00000433054.1:n.*126T>A
ENST00000532399.1:n.989T>A
NM_002496.3:c.284T>A	NP_002487.1:p.Phe95Tyr
XM_005274013.1:c.284T>A	XP_005274070.1:p.Phe95Tyr
XM_005274014.1:c.284T>A	XP_005274071.1:p.Phe95Tyr
XM_005274015.1:c.164T>A	XP_005274072.1:p.Phe55Tyr
XM_011545053.1:c.284T>A	XP_011543355.1:p.Phe95Tyr
NM_002496.4:c.284T>A MANE Select	NP_002487.1:p.Phe95Tyr