Canonical Allele Identifier: CA2172237551
Gene: NDUFAF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.41396188_41396189delinsCT , CM000677.2:g.41396188_41396189delinsCT GRCh38
NC_000015.9:g.41688386_41688387delinsCT , CM000677.1:g.41688386_41688387delinsCT GRCh37
NC_000015.8:g.39475678_39475679delinsCT NCBI36
NG_031924.1:g.11272_11273delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000260361.9:c.573+298_573+299delinsAG MANE Select ENSP00000260361.4:n.573+298_573+299delinsAG
ENST00000558719.2:c.573+298_573+299delinsAG ENSP00000454083.2:n.573+298_573+299delinsAG
ENST00000560978.2:c.573+298_573+299delinsAG ENSP00000453944.2:n.573+298_573+299delinsAG
ENST00000676533.1:c.573+298_573+299delinsAG ENSP00000504040.1:n.573+298_573+299delinsAG
ENST00000676906.1:c.114+298_114+299delinsAG ENSP00000503122.1:n.114+298_114+299delinsAG
ENST00000677477.1:n.1799+298_1799+299delinsAG
ENST00000678029.1:c.573+298_573+299delinsAG ENSP00000503887.1:n.573+298_573+299delinsAG
ENST00000678745.1:c.573+298_573+299delinsAG ENSP00000503632.1:n.573+298_573+299delinsAG
ENST00000679094.1:c.573+298_573+299delinsAG ENSP00000504295.1:n.573+298_573+299delinsAG
ENST00000679240.1:n.971+298_971+299delinsAG
ENST00000260361.8:c.573+298_573+299delinsAG ENSP00000260361.4:n.573+298_573+299delinsAG
ENST00000559127.5:c.573+298_573+299delinsAG ENSP00000453027.1:n.573+298_573+299delinsAG
ENST00000560978.1:c.573+298_573+299delinsAG ENSP00000453944.1:n.573+298_573+299delinsAG
NM_016013.3:c.573+298_573+299delinsAG NP_057097.2:n.573+298_573+299delinsAG
NR_045620.1:n.971+298_971+299delinsAG
XM_006720555.1:c.573+298_573+299delinsAG XP_006720618.1:n.573+298_573+299delinsAG
XM_011521658.1:c.573+298_573+299delinsAG XP_011519960.1:n.573+298_573+299delinsAG
XM_011521659.1:c.573+298_573+299delinsAG XP_011519961.1:n.573+298_573+299delinsAG
XM_006720555.3:c.573+298_573+299delinsAG XP_006720618.1:n.573+298_573+299delinsAG
XM_011521659.3:c.573+298_573+299delinsAG XP_011519961.1:n.573+298_573+299delinsAG
XM_024449945.1:c.573+298_573+299delinsAG XP_024305713.1:n.573+298_573+299delinsAG
NM_016013.4:c.573+298_573+299delinsAG MANE Select NP_057097.2:n.573+298_573+299delinsAG
NR_045620.2:n.1007+298_1007+299delinsAG