Canonical Allele Identifier: CA617563575
Gene: NDUFAF1 HGNC NCBI

Linked Data

dbSNP Id: rs1373976298

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.41396401_41396403del , CM000677.2:g.41396401_41396403del GRCh38
NC_000015.9:g.41688599_41688601del , CM000677.1:g.41688599_41688601del GRCh37
NC_000015.8:g.39475891_39475893del NCBI36
NG_031924.1:g.11059_11061del

Transcript Alleles

HGVS Amino-acid Change
ENST00000260361.9:c.573+85_573+87del MANE Select ENSP00000260361.4:n.573+85_573+87del
ENST00000558719.2:c.573+85_573+87del ENSP00000454083.2:n.573+85_573+87del
ENST00000560978.2:c.573+85_573+87del ENSP00000453944.2:n.573+85_573+87del
ENST00000676533.1:c.573+85_573+87del ENSP00000504040.1:n.573+85_573+87del
ENST00000676906.1:c.114+85_114+87del ENSP00000503122.1:n.114+85_114+87del
ENST00000677477.1:n.1799+85_1799+87del
ENST00000678029.1:c.573+85_573+87del ENSP00000503887.1:n.573+85_573+87del
ENST00000678745.1:c.573+85_573+87del ENSP00000503632.1:n.573+85_573+87del
ENST00000679094.1:c.573+85_573+87del ENSP00000504295.1:n.573+85_573+87del
ENST00000679240.1:n.971+85_971+87del
ENST00000260361.8:c.573+85_573+87del ENSP00000260361.4:n.573+85_573+87del
ENST00000559127.5:c.573+85_573+87del ENSP00000453027.1:n.573+85_573+87del
ENST00000560978.1:c.573+85_573+87del ENSP00000453944.1:n.573+85_573+87del
NM_016013.3:c.573+85_573+87del NP_057097.2:n.573+85_573+87del
NR_045620.1:n.971+85_971+87del
XM_006720555.1:c.573+85_573+87del XP_006720618.1:n.573+85_573+87del
XM_011521658.1:c.573+85_573+87del XP_011519960.1:n.573+85_573+87del
XM_011521659.1:c.573+85_573+87del XP_011519961.1:n.573+85_573+87del
XM_006720555.3:c.573+85_573+87del XP_006720618.1:n.573+85_573+87del
XM_011521659.3:c.573+85_573+87del XP_011519961.1:n.573+85_573+87del
XM_024449945.1:c.573+85_573+87del XP_024305713.1:n.573+85_573+87del
NM_016013.4:c.573+85_573+87del MANE Select NP_057097.2:n.573+85_573+87del
NR_045620.2:n.1007+85_1007+87del