Canonical Allele Identifier: CA2172237335

Gene: NDUFAF1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.41395954_41395956delinsGGT , CM000677.2:g.41395954_41395956delinsGGT	GRCh38
NC_000015.9:g.41688152_41688154delinsGGT , CM000677.1:g.41688152_41688154delinsGGT	GRCh37
NC_000015.8:g.39475444_39475446delinsGGT	NCBI36
NG_031924.1:g.11505_11507delinsACC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260361.9:c.573+531_573+533delinsACC MANE Select	ENSP00000260361.4:n.573+531_573+533delinsACC
ENST00000558719.2:c.573+531_573+533delinsACC	ENSP00000454083.2:n.573+531_573+533delinsACC
ENST00000560978.2:c.573+531_573+533delinsACC	ENSP00000453944.2:n.573+531_573+533delinsACC
ENST00000676533.1:c.573+531_573+533delinsACC	ENSP00000504040.1:n.573+531_573+533delinsACC
ENST00000676906.1:c.114+531_114+533delinsACC	ENSP00000503122.1:n.114+531_114+533delinsACC
ENST00000677477.1:n.1799+531_1799+533delinsACC
ENST00000678029.1:c.573+531_573+533delinsACC	ENSP00000503887.1:n.573+531_573+533delinsACC
ENST00000678745.1:c.573+531_573+533delinsACC	ENSP00000503632.1:n.573+531_573+533delinsACC
ENST00000679094.1:c.573+531_573+533delinsACC	ENSP00000504295.1:n.573+531_573+533delinsACC
ENST00000679240.1:n.971+531_971+533delinsACC
ENST00000260361.8:c.573+531_573+533delinsACC	ENSP00000260361.4:n.573+531_573+533delinsACC
ENST00000559127.5:c.573+531_573+533delinsACC	ENSP00000453027.1:n.573+531_573+533delinsACC
ENST00000560978.1:c.573+531_573+533delinsACC	ENSP00000453944.1:n.573+531_573+533delinsACC
NM_016013.3:c.573+531_573+533delinsACC	NP_057097.2:n.573+531_573+533delinsACC
NR_045620.1:n.971+531_971+533delinsACC
XM_006720555.1:c.573+531_573+533delinsACC	XP_006720618.1:n.573+531_573+533delinsACC
XM_011521658.1:c.573+531_573+533delinsACC	XP_011519960.1:n.573+531_573+533delinsACC
XM_011521659.1:c.573+531_573+533delinsACC	XP_011519961.1:n.573+531_573+533delinsACC
XM_006720555.3:c.573+531_573+533delinsACC	XP_006720618.1:n.573+531_573+533delinsACC
XM_011521659.3:c.573+531_573+533delinsACC	XP_011519961.1:n.573+531_573+533delinsACC
XM_024449945.1:c.573+531_573+533delinsACC	XP_024305713.1:n.573+531_573+533delinsACC
NM_016013.4:c.573+531_573+533delinsACC MANE Select	NP_057097.2:n.573+531_573+533delinsACC
NR_045620.2:n.1007+531_1007+533delinsACC