Canonical Allele Identifier: CA3045837305
Gene: NDUFV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67611984_67611985insCCGATTTGTGAAGGGAGATGCCCGGCCAGCTGAGATTGACTCCCTGTGGGAGATCAGCAAGCAGATAGA , CM000673.2:g.67611984_67611985insCCGATTTGTGAAGGGAGATGCCCGGCCAGCTGAGATTGACTCCCTGTGGGAGATCAGCAAGCAGATAGA GRCh38
NC_000011.9:g.67379455_67379456insCCGATTTGTGAAGGGAGATGCCCGGCCAGCTGAGATTGACTCCCTGTGGGAGATCAGCAAGCAGATAGA , CM000673.1:g.67379455_67379456insCCGATTTGTGAAGGGAGATGCCCGGCCAGCTGAGATTGACTCCCTGTGGGAGATCAGCAAGCAGATAGA GRCh37
NC_000011.8:g.67136031_67136032insCCGATTTGTGAAGGGAGATGCCCGGCCAGCTGAGATTGACTCCCTGTGGGAGATCAGCAAGCAGATAGA NCBI36
NG_013353.1:g.10133_10134insCCGATTTGTGAAGGGAGATGCCCGGCCAGCTGAGATTGACTCCCTGTGGGAGATCAGCAAGCAGATAGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000322776.11:c.1162+6_1162+7insCCGATTTGTGAAGGGAGATGCCCGGCCAGCTGAGATTGACTCCCTGTGGGAGATCAGCAAGCAGATAGA MANE Select ENSP00000322450.6:n.1162+6_1162+7insCCGATTTGTGAAGGGAGATGCCCGG...
ENST00000647561.1:c.1162+6_1162+7insCCGATTTGTGAAGGGAGATGCCCGGCCAGCTGAGATTGACTCCCTGTGGGAGATCAGCAAGCAGATAGA ENSP00000497587.1:n.1162+6_1162+7insCCGATTTGTGAAGGGAGATGCCCGG...
ENST00000322776.10:c.1162+6_1162+7insCCGATTTGTGAAGGGAGATGCCCGGCCAGCTGAGATTGACTCCCTGTGGGAGATCAGCAAGCAGATAGA ENSP00000322450.6:n.1162+6_1162+7insCCGATTTGTGAAGGGAGATGCCCGG...
ENST00000415352.6:c.1141+6_1141+7insCCGATTTGTGAAGGGAGATGCCCGGCCAGCTGAGATTGACTCCCTGTGGGAGATCAGCAAGCAGATAGA ENSP00000395368.2:n.1141+6_1141+7insCCGATTTGTGAAGGGAGATGCCCGG...
ENST00000526770.5:n.1445+6_1445+7insCCGATTTGTGAAGGGAGATGCCCGGCCAGCTGAGATTGACTCCCTGTGGGAGATCAGCAAGCAGATAGA
ENST00000527355.5:c.370-136_370-135insCCGATTTGTGAAGGGAGATGCCCGGCCAGCTGAGATTGACTCCCTGTGGGAGATCAGCAAGCAGATAGA ENSP00000432637.1:n.370-136_370-135insCCGATTTGTGAAGGGAGATGCCC...
ENST00000527923.1:n.504+6_504+7insCCGATTTGTGAAGGGAGATGCCCGGCCAGCTGAGATTGACTCCCTGTGGGAGATCAGCAAGCAGATAGA
ENST00000529927.5:c.1135+6_1135+7insCCGATTTGTGAAGGGAGATGCCCGGCCAGCTGAGATTGACTCCCTGTGGGAGATCAGCAAGCAGATAGA ENSP00000436766.1:n.1135+6_1135+7insCCGATTTGTGAAGGGAGATGCCCGG...
ENST00000531250.1:n.426+6_426+7insCCGATTTGTGAAGGGAGATGCCCGGCCAGCTGAGATTGACTCCCTGTGGGAGATCAGCAAGCAGATAGA
ENST00000532303.5:c.859+6_859+7insCCGATTTGTGAAGGGAGATGCCCGGCCAGCTGAGATTGACTCCCTGTGGGAGATCAGCAAGCAGATAGA ENSP00000432015.1:n.859+6_859+7insCCGATTTGTGAAGGGAGATGCCCGGCC...
ENST00000533919.5:c.566+6_566+7insCCGATTTGTGAAGGGAGATGCCCGGCCAGCTGAGATTGACTCCCTGTGGGAGATCAGCAAGCAGATAGA ENSP00000435199.1:n.566+6_566+7insCCGATTTGTGAAGGGAGATGCCCGGCC...
ENST00000534352.1:n.266_267insCCGATTTGTGAAGGGAGATGCCCGGCCAGCTGAGATTGACTCCCTGTGGGAGATCAGCAAGCAGATAGA
NM_001166102.1:c.1135+6_1135+7insCCGATTTGTGAAGGGAGATGCCCGGCCAGCTGAGATTGACTCCCTGTGGGAGATCAGCAAGCAGATAGA NP_001159574.1:n.1135+6_1135+7insCCGATTTGTGAAGGGAGATGCCCGGCCA...
NM_007103.3:c.1162+6_1162+7insCCGATTTGTGAAGGGAGATGCCCGGCCAGCTGAGATTGACTCCCTGTGGGAGATCAGCAAGCAGATAGA NP_009034.2:n.1162+6_1162+7insCCGATTTGTGAAGGGAGATGCCCGGCCAGCT...
NM_001166102.2:c.1135+6_1135+7insCCGATTTGTGAAGGGAGATGCCCGGCCAGCTGAGATTGACTCCCTGTGGGAGATCAGCAAGCAGATAGA NP_001159574.1:n.1135+6_1135+7insCCGATTTGTGAAGGGAGATGCCCGGCCA...
NM_007103.4:c.1162+6_1162+7insCCGATTTGTGAAGGGAGATGCCCGGCCAGCTGAGATTGACTCCCTGTGGGAGATCAGCAAGCAGATAGA MANE Select NP_009034.2:n.1162+6_1162+7insCCGATTTGTGAAGGGAGATGCCCGGCCAGCT...