Canonical Allele Identifier: CA381599957
Gene: NDUFS8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68033205G>C , CM000673.2:g.68033205G>C GRCh38
NC_000011.9:g.67800672G>C , CM000673.1:g.67800672G>C GRCh37
NC_000011.8:g.67557248G>C NCBI36
NG_017040.1:g.7589G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000313468.10:c.294G>C MANE Select ENSP00000315774.5:p.Glu98Asp
ENST00000313468.9:c.294G>C ENSP00000315774.5:p.Glu98Asp
ENST00000432321.6:n.411G>C
ENST00000453471.6:c.294G>C ENSP00000403972.2:p.Glu98Asp
ENST00000524810.5:c.65G>C
ENST00000525419.5:c.240G>C ENSP00000433521.1:p.Glu80Asp
ENST00000525628.1:c.294G>C ENSP00000432968.1:p.Glu98Asp
ENST00000526339.5:c.294G>C ENSP00000436287.1:p.Glu98Asp
ENST00000526446.5:c.*349G>C ENSP00000433645.1:n.*349G>C
ENST00000528492.1:c.-67+2472G>C ENSP00000432848.1:n.-67+2472G>C
ENST00000529645.1:c.472G>C ENSP00000431293.1:n.472G>C
ENST00000531228.1:c.*136G>C ENSP00000433054.1:n.*136G>C
ENST00000532399.1:n.999G>C
NM_002496.3:c.294G>C NP_002487.1:p.Glu98Asp
XM_005274013.1:c.294G>C XP_005274070.1:p.Glu98Asp
XM_005274014.1:c.294G>C XP_005274071.1:p.Glu98Asp
XM_005274015.1:c.174G>C XP_005274072.1:p.Glu58Asp
XM_011545053.1:c.294G>C XP_011543355.1:p.Glu98Asp
NM_002496.4:c.294G>C MANE Select NP_002487.1:p.Glu98Asp