Canonical Allele Identifier: CA939089292
Gene: NDUFS8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68033282_68033283insATCACGATCGAAAGCGATGTGCGCGGCGACGGCAGCCGCCGCACGACGCGTTACGACATCGACCTGACCAAGTGCATCTTCTGCGGCTTCTGCGAAGAGAGCTGCCC , CM000673.2:g.68033282_68033283insATCACGATCGAAAGCGATGTGCGCGGCGACGGCAGCCGCCGCACGACGCGTTACGACATCGACCTGACCAAGTGCATCTTCTGCGGCTTCTGCGAAGAGAGCTGCCC GRCh38
NC_000011.9:g.67800749_67800750insATCACGATCGAAAGCGATGTGCGCGGCGACGGCAGCCGCCGCACGACGCGTTACGACATCGACCTGACCAAGTGCATCTTCTGCGGCTTCTGCGAAGAGAGCTGCCC , CM000673.1:g.67800749_67800750insATCACGATCGAAAGCGATGTGCGCGGCGACGGCAGCCGCCGCACGACGCGTTACGACATCGACCTGACCAAGTGCATCTTCTGCGGCTTCTGCGAAGAGAGCTGCCC GRCh37
NC_000011.8:g.67557325_67557326insATCACGATCGAAAGCGATGTGCGCGGCGACGGCAGCCGCCGCACGACGCGTTACGACATCGACCTGACCAAGTGCATCTTCTGCGGCTTCTGCGAAGAGAGCTGCCC NCBI36
NG_017040.1:g.7666_7667insATCACGATCGAAAGCGATGTGCGCGGCGACGGCAGCCGCCGCACGACGCGTTACGACATCGACCTGACCAAGTGCATCTTCTGCGGCTTCTGCGAAGAGAGCTGCCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000313468.10:c.371_372insATCACGATCGAAAGCGATGTGCGCGGCGACGGCAGCCGCCGCACGACGCGTTACGACATCGACCTGACCAAGTGCATCTTCTGCGGCTTCTGCGAAGAGAGCTGCCC MANE Select ENSP00000315774.5:p.Ala125SerfsTer22
ENST00000313468.9:c.371_372insATCACGATCGAAAGCGATGTGCGCGGCGACGGCAGCCGCCGCACGACGCGTTACGACATCGACCTGACCAAGTGCATCTTCTGCGGCTTCTGCGAAGAGAGCTGCCC ENSP00000315774.5:p.Ala125SerfsTer22
ENST00000432321.6:n.488_489insATCACGATCGAAAGCGATGTGCGCGGCGACGGCAGCCGCCGCACGACGCGTTACGACATCGACCTGACCAAGTGCATCTTCTGCGGCTTCTGCGAAGAGAGCTGCCC
ENST00000453471.6:c.371_372insATCACGATCGAAAGCGATGTGCGCGGCGACGGCAGCCGCCGCACGACGCGTTACGACATCGACCTGACCAAGTGCATCTTCTGCGGCTTCTGCGAAGAGAGCTGCCC ENSP00000403972.2:p.Gln124=
ENST00000524810.5:c.142_143insATCACGATCGAAAGCGATGTGCGCGGCGACGGCAGCCGCCGCACGACGCGTTACGACATCGACCTGACCAAGTGCATCTTCTGCGGCTTCTGCGAAGAGAGCTGCCC
ENST00000525419.5:c.317_318insATCACGATCGAAAGCGATGTGCGCGGCGACGGCAGCCGCCGCACGACGCGTTACGACATCGACCTGACCAAGTGCATCTTCTGCGGCTTCTGCGAAGAGAGCTGCCC ENSP00000433521.1:p.Ala107SerfsTer22
ENST00000526339.5:c.371_372insATCACGATCGAAAGCGATGTGCGCGGCGACGGCAGCCGCCGCACGACGCGTTACGACATCGACCTGACCAAGTGCATCTTCTGCGGCTTCTGCGAAGAGAGCTGCCC ENSP00000436287.1:p.Ala125SerfsTer22
ENST00000526446.5:c.*426_*427insATCACGATCGAAAGCGATGTGCGCGGCGACGGCAGCCGCCGCACGACGCGTTACGACATCGACCTGACCAAGTGCATCTTCTGCGGCTTCTGCGAAGAGAGCTGCCC ENSP00000433645.1:n.*426_*427insATCACGATCGAAAGCGATGTGCGCGGCGA...
ENST00000528492.1:c.-67+2549_-67+2550insATCACGATCGAAAGCGATGTGCGCGGCGACGGCAGCCGCCGCACGACGCGTTACGACATCGACCTGACCAAGTGCATCTTCTGCGGCTTCTGCGAAGAGAGCTGCCC ENSP00000432848.1:n.-67+2549_-67+2550insATCACGATCGAAAGCGATGTG...
ENST00000529645.1:c.549_550insATCACGATCGAAAGCGATGTGCGCGGCGACGGCAGCCGCCGCACGACGCGTTACGACATCGACCTGACCAAGTGCATCTTCTGCGGCTTCTGCGAAGAGAGCTGCCC ENSP00000431293.1:n.549_550insATCACGATCGAAAGCGATGTGCGCGGCGACG...
ENST00000532399.1:n.1076_1077insATCACGATCGAAAGCGATGTGCGCGGCGACGGCAGCCGCCGCACGACGCGTTACGACATCGACCTGACCAAGTGCATCTTCTGCGGCTTCTGCGAAGAGAGCTGCCC
NM_002496.3:c.371_372insATCACGATCGAAAGCGATGTGCGCGGCGACGGCAGCCGCCGCACGACGCGTTACGACATCGACCTGACCAAGTGCATCTTCTGCGGCTTCTGCGAAGAGAGCTGCCC NP_002487.1:p.Ala125SerfsTer22
XM_005274013.1:c.371_372insATCACGATCGAAAGCGATGTGCGCGGCGACGGCAGCCGCCGCACGACGCGTTACGACATCGACCTGACCAAGTGCATCTTCTGCGGCTTCTGCGAAGAGAGCTGCCC XP_005274070.1:p.Ala125SerfsTer22
XM_005274014.1:c.371_372insATCACGATCGAAAGCGATGTGCGCGGCGACGGCAGCCGCCGCACGACGCGTTACGACATCGACCTGACCAAGTGCATCTTCTGCGGCTTCTGCGAAGAGAGCTGCCC XP_005274071.1:p.Ala125SerfsTer22
XM_005274015.1:c.251_252insATCACGATCGAAAGCGATGTGCGCGGCGACGGCAGCCGCCGCACGACGCGTTACGACATCGACCTGACCAAGTGCATCTTCTGCGGCTTCTGCGAAGAGAGCTGCCC XP_005274072.1:p.Ala85SerfsTer22
XM_011545053.1:c.371_372insATCACGATCGAAAGCGATGTGCGCGGCGACGGCAGCCGCCGCACGACGCGTTACGACATCGACCTGACCAAGTGCATCTTCTGCGGCTTCTGCGAAGAGAGCTGCCC XP_011543355.1:p.Ala125SerfsTer22
NM_002496.4:c.371_372insATCACGATCGAAAGCGATGTGCGCGGCGACGGCAGCCGCCGCACGACGCGTTACGACATCGACCTGACCAAGTGCATCTTCTGCGGCTTCTGCGAAGAGAGCTGCCC MANE Select NP_002487.1:p.Ala125SerfsTer22