Canonical Allele Identifier: CA7491270
Gene: NDUFAF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.41394887C>T , CM000677.2:g.41394887C>T GRCh38
NC_000015.9:g.41687085C>T , CM000677.1:g.41687085C>T GRCh37
NC_000015.8:g.39474377C>T NCBI36
NG_031924.1:g.12574G>A

Transcript Alleles

HGVS Amino-acid Change
NM_016013.4:c.731G>A MANE Select NP_057097.2:p.Arg244His
ENST00000260361.9:c.731G>A MANE Select ENSP00000260361.4:p.Arg244His
NM_016013.3:c.731G>A NP_057097.2:p.Arg244His
NR_045620.1:n.1129G>A
NR_045620.2:n.1165G>A
ENST00000260361.8:c.731G>A ENSP00000260361.4:p.Arg244His
ENST00000558719.2:c.731G>A ENSP00000454083.2:p.Arg244His
ENST00000559127.5:c.731G>A ENSP00000453027.1:p.Arg244His
ENST00000560978.2:c.731G>A ENSP00000453944.2:p.Arg244His
ENST00000676533.1:c.731G>A ENSP00000504040.1:p.Arg244His
ENST00000676906.1:c.272G>A ENSP00000503122.1:p.Arg91His
ENST00000677477.1:n.1957G>A
ENST00000678029.1:c.731G>A ENSP00000503887.1:p.Arg244His
ENST00000678745.1:c.731G>A ENSP00000503632.1:p.Arg244His
ENST00000679094.1:c.731G>A ENSP00000504295.1:p.Arg244His
ENST00000679240.1:n.1129G>A
XM_006720555.1:c.731G>A XP_006720618.1:p.Arg244His
XM_006720555.3:c.731G>A XP_006720618.1:p.Arg244His
XM_011521658.1:c.731G>A XP_011519960.1:p.Arg244His
XM_011521659.1:c.731G>A XP_011519961.1:p.Arg244His
XM_011521659.3:c.731G>A XP_011519961.1:p.Arg244His
XM_024449945.1:c.731G>A XP_024305713.1:p.Arg244His