Canonical Allele Identifier: CA462299227

Gene: NDUFAF6

Linked Data

• gnomAD v4: 8-95025113-G-T
• MyVariant Identifiers: chr8:g.96037341G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.95025113G>T , CM000670.2:g.95025113G>T	GRCh38
NC_000008.10:g.96037341G>T , CM000670.1:g.96037341G>T	GRCh37
NC_000008.9:g.96106517G>T	NCBI36
NG_016647.1:g.5121G>T
NG_016647.2:g.134843G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000519804.2:c.105G>T	ENSP00000430230.2:p.Arg35=
ENST00000697355.1:c.-83-6882G>T	ENSP00000513277.1:n.-83-6882G>T
ENST00000697364.1:c.-83-6882G>T	ENSP00000513278.1:n.-83-6882G>T
ENST00000396124.9:c.105G>T MANE Select	ENSP00000379430.4:p.Arg35=
ENST00000396111.6:c.-83-6882G>T	ENSP00000379417.1:n.-83-6882G>T
ENST00000396113.5:c.-84+1794G>T	ENSP00000379419.1:n.-84+1794G>T
ENST00000396124.8:c.105G>T	ENSP00000379430.4:p.Arg35=
ENST00000454358.6:c.46G>T
ENST00000517976.5:c.93G>T	ENSP00000430099.1:p.Arg31=
ENST00000518258.5:c.105G>T	ENSP00000428788.1:p.Arg35=
ENST00000518608.5:c.46G>T
ENST00000519136.5:c.-255-6882G>T	ENSP00000429585.1:n.-255-6882G>T
ENST00000520632.5:c.81G>T	ENSP00000428666.1:p.Arg27=
ENST00000520757.1:c.46G>T
ENST00000522683.5:c.48G>T	ENSP00000430991.1:p.Arg16=
ENST00000523337.5:c.105G>T	ENSP00000429038.1:p.Arg35=
ENST00000523378.5:c.-83-6882G>T	ENSP00000428034.1:n.-83-6882G>T
NM_152416.3:c.105G>T	NP_689629.2:p.Arg35=
XM_005250789.1:c.-176G>T	XP_005250846.1:n.-176G>T
XM_005250790.1:c.-348G>T	XP_005250847.1:n.-348G>T
XM_005250791.1:c.-476G>T	XP_005250848.1:n.-476G>T
XM_005250792.1:c.-480G>T	XP_005250849.1:n.-480G>T
XM_011516833.1:c.42-6882G>T	XP_011515135.1:n.42-6882G>T
XM_011516834.1:c.42-6882G>T	XP_011515136.1:n.42-6882G>T
XM_011516835.1:c.42-6882G>T	XP_011515137.1:n.42-6882G>T
XM_011516836.1:c.42-6882G>T	XP_011515138.1:n.42-6882G>T
XM_011516837.1:c.42-6882G>T	XP_011515139.1:n.42-6882G>T
XM_011516838.1:c.42-6882G>T	XP_011515140.1:n.42-6882G>T
XM_011516839.1:c.42-6882G>T	XP_011515141.1:n.42-6882G>T
XM_011516840.1:c.42-6882G>T	XP_011515142.1:n.42-6882G>T
XM_011516841.1:c.42-6882G>T	XP_011515143.1:n.42-6882G>T
XM_011516842.1:c.42-6882G>T	XP_011515144.1:n.42-6882G>T
XM_011516843.1:c.-84+1794G>T	XP_011515145.1:n.-84+1794G>T
NM_001330582.1:c.-176G>T	NP_001317511.1:n.-176G>T
NM_001354514.1:c.-83-6882G>T	NP_001341443.1:n.-83-6882G>T
NM_001354515.1:c.-83-6882G>T	NP_001341444.1:n.-83-6882G>T
NM_001354516.1:c.42-6882G>T	NP_001341445.1:n.42-6882G>T
NM_001354517.1:c.-129G>T	NP_001341446.1:n.-129G>T
NM_001354518.1:c.-348G>T	NP_001341447.1:n.-348G>T
NM_001354519.1:c.-344G>T	NP_001341448.1:n.-344G>T
NM_001354521.1:c.-176G>T	NP_001341450.1:n.-176G>T
NM_001354522.1:c.-383-6882G>T	NP_001341451.1:n.-383-6882G>T
NM_001354524.1:c.-456-6882G>T	NP_001341453.1:n.-456-6882G>T
NM_001354525.1:c.-456-6882G>T	NP_001341454.1:n.-456-6882G>T
NM_001354527.1:c.-693G>T	NP_001341456.1:n.-693G>T
NM_001354528.1:c.-664G>T	NP_001341457.1:n.-664G>T
NM_001354529.1:c.-476G>T	NP_001341458.1:n.-476G>T
NM_001354530.1:c.-578G>T	NP_001341459.1:n.-578G>T
NM_001354531.1:c.-574G>T	NP_001341460.1:n.-574G>T
NM_001354532.1:c.-582G>T	NP_001341461.1:n.-582G>T
NM_001354533.1:c.-545G>T	NP_001341462.1:n.-545G>T
NM_001354534.1:c.-136-6882G>T	NP_001341463.1:n.-136-6882G>T
NR_148910.1:n.139G>T
NR_148911.1:n.139G>T
NR_148912.1:n.139G>T
NR_148913.1:n.139G>T
NR_148914.1:n.139G>T
NR_148915.1:n.139G>T
XM_005250792.2:c.-480G>T	XP_005250849.1:n.-480G>T
XM_005250793.3:c.-549G>T	XP_005250850.1:n.-549G>T
XM_011516833.2:c.42-6882G>T	XP_011515135.1:n.42-6882G>T
XM_011516834.2:c.42-6882G>T	XP_011515136.1:n.42-6882G>T
XM_011516835.2:c.42-6882G>T	XP_011515137.1:n.42-6882G>T
XM_011516836.2:c.42-6882G>T	XP_011515138.1:n.42-6882G>T
XM_011516837.2:c.42-6882G>T	XP_011515139.1:n.42-6882G>T
XM_011516838.2:c.42-6882G>T	XP_011515140.1:n.42-6882G>T
XM_011516839.2:c.42-6882G>T	XP_011515141.1:n.42-6882G>T
XM_011516840.2:c.42-6882G>T	XP_011515142.1:n.42-6882G>T
XM_011516841.2:c.42-6882G>T	XP_011515143.1:n.42-6882G>T
XM_011516842.2:c.42-6882G>T	XP_011515144.1:n.42-6882G>T
XM_017013027.2:c.42-6882G>T	XP_016868516.1:n.42-6882G>T
XM_017013028.1:c.42-6882G>T	XP_016868517.1:n.42-6882G>T
XM_017013029.1:c.42-6882G>T	XP_016868518.1:n.42-6882G>T
XM_017013033.2:c.-84+1794G>T	XP_016868522.1:n.-84+1794G>T
XM_024447062.1:c.-136-6882G>T	XP_024302830.1:n.-136-6882G>T
NM_152416.4:c.105G>T MANE Select	NP_689629.2:p.Arg35=
NR_148913.2:n.125G>T
NR_148914.2:n.125G>T
NM_001330582.2:c.-176G>T	NP_001317511.1:n.-176G>T
NM_001354514.2:c.-83-6882G>T	NP_001341443.1:n.-83-6882G>T
NM_001354515.2:c.-83-6882G>T	NP_001341444.1:n.-83-6882G>T
NM_001354516.2:c.42-6882G>T	NP_001341445.1:n.42-6882G>T
NM_001354517.2:c.-129G>T	NP_001341446.1:n.-129G>T
NM_001354518.2:c.-348G>T	NP_001341447.1:n.-348G>T
NM_001354519.2:c.-344G>T	NP_001341448.1:n.-344G>T
NM_001354521.2:c.-176G>T	NP_001341450.1:n.-176G>T
NM_001354522.2:c.-383-6882G>T	NP_001341451.1:n.-383-6882G>T
NM_001354524.2:c.-456-6882G>T	NP_001341453.1:n.-456-6882G>T
NM_001354525.2:c.-456-6882G>T	NP_001341454.1:n.-456-6882G>T
NM_001354527.2:c.-693G>T	NP_001341456.1:n.-693G>T
NM_001354528.2:c.-664G>T	NP_001341457.1:n.-664G>T
NM_001354529.2:c.-476G>T	NP_001341458.1:n.-476G>T
NM_001354530.2:c.-578G>T	NP_001341459.1:n.-578G>T
NM_001354531.2:c.-574G>T	NP_001341460.1:n.-574G>T
NM_001354532.2:c.-582G>T	NP_001341461.1:n.-582G>T
NM_001354533.2:c.-545G>T	NP_001341462.1:n.-545G>T
NM_001354534.2:c.-136-6882G>T	NP_001341463.1:n.-136-6882G>T
NR_148910.2:n.125G>T
NR_148911.2:n.125G>T
NR_148912.2:n.125G>T
NR_148915.2:n.125G>T