Canonical Allele Identifier: CA2614684239
Gene: NDUFS8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68033094_68033095insGGCCTGGGTG , CM000673.2:g.68033094_68033095insGGCCTGGGTG GRCh38
NC_000011.9:g.67800561_67800562insGGCCTGGGTG , CM000673.1:g.67800561_67800562insGGCCTGGGTG GRCh37
NC_000011.8:g.67557137_67557138insGGCCTGGGTG NCBI36
NG_017040.1:g.7478_7479insGGCCTGGGTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000313468.10:c.200-17_200-16insGGCCTGGGTG MANE Select ENSP00000315774.5:n.200-17_200-16insGGCCTGGGTG
ENST00000313468.9:c.200-17_200-16insGGCCTGGGTG ENSP00000315774.5:n.200-17_200-16insGGCCTGGGTG
ENST00000432321.6:n.317-17_317-16insGGCCTGGGTG
ENST00000453471.6:c.200-17_200-16insGGCCTGGGTG ENSP00000403972.2:n.200-17_200-16insGGCCTGGGTG
ENST00000525419.5:c.146-17_146-16insGGCCTGGGTG ENSP00000433521.1:n.146-17_146-16insGGCCTGGGTG
ENST00000525628.1:c.200-17_200-16insGGCCTGGGTG ENSP00000432968.1:n.200-17_200-16insGGCCTGGGTG
ENST00000526339.5:c.200-17_200-16insGGCCTGGGTG ENSP00000436287.1:n.200-17_200-16insGGCCTGGGTG
ENST00000526446.5:c.*255-17_*255-16insGGCCTGGGTG ENSP00000433645.1:n.*255-17_*255-16insGGCCTGGGTG
ENST00000528492.1:c.-67+2361_-67+2362insGGCCTGGGTG ENSP00000432848.1:n.-67+2361_-67+2362insGGCCTGGGTG
ENST00000529645.1:c.378-17_378-16insGGCCTGGGTG ENSP00000431293.1:n.378-17_378-16insGGCCTGGGTG
ENST00000531228.1:c.*42-17_*42-16insGGCCTGGGTG ENSP00000433054.1:n.*42-17_*42-16insGGCCTGGGTG
ENST00000532399.1:n.888_889insGGCCTGGGTG
NM_002496.3:c.200-17_200-16insGGCCTGGGTG NP_002487.1:n.200-17_200-16insGGCCTGGGTG
XM_005274013.1:c.200-17_200-16insGGCCTGGGTG XP_005274070.1:n.200-17_200-16insGGCCTGGGTG
XM_005274014.1:c.200-17_200-16insGGCCTGGGTG XP_005274071.1:n.200-17_200-16insGGCCTGGGTG
XM_005274015.1:c.80-17_80-16insGGCCTGGGTG XP_005274072.1:n.80-17_80-16insGGCCTGGGTG
XM_011545053.1:c.200-17_200-16insGGCCTGGGTG XP_011543355.1:n.200-17_200-16insGGCCTGGGTG
NM_002496.4:c.200-17_200-16insGGCCTGGGTG MANE Select NP_002487.1:n.200-17_200-16insGGCCTGGGTG