Canonical Allele Identifier: CA2663931183

Gene: NDUFA10

Linked Data

• gnomAD v4: 2-240014602-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.240014602C>A , CM000664.2:g.240014602C>A	GRCh38
NC_000002.11:g.240954019C>A , CM000664.1:g.240954019C>A	GRCh37
NC_000002.10:g.240602692C>A	NCBI36
NG_031855.1:g.15801G>T
NG_031855.2:g.15801G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252711.7:c.669+137G>T MANE Select	ENSP00000252711.2:n.669+137G>T
ENST00000414580.2:c.*352G>T	ENSP00000388413.2:n.*352G>T
ENST00000444548.6:c.669+137G>T	ENSP00000403080.2:n.669+137G>T
ENST00000448880.6:c.669+137G>T	ENSP00000408224.2:n.669+137G>T
ENST00000476216.6:n.903G>T
ENST00000620965.5:c.669+137G>T	ENSP00000480897.2:n.669+137G>T
ENST00000676491.1:c.669+137G>T	ENSP00000504528.1:n.669+137G>T
ENST00000676782.1:c.669+137G>T	ENSP00000504717.1:n.669+137G>T
ENST00000676784.1:n.892G>T
ENST00000676929.1:c.669+137G>T	ENSP00000503956.1:n.669+137G>T
ENST00000677057.1:n.902G>T
ENST00000677114.1:c.547+3951G>T	ENSP00000504818.1:n.547+3951G>T
ENST00000677155.1:c.547+3951G>T	ENSP00000502921.1:n.547+3951G>T
ENST00000677263.1:c.669+137G>T	ENSP00000503790.1:n.669+137G>T
ENST00000677294.1:c.639+167G>T	ENSP00000503461.1:n.639+167G>T
ENST00000677368.1:c.547+3951G>T	ENSP00000502983.1:n.547+3951G>T
ENST00000677395.1:c.*95G>T	ENSP00000502890.1:n.*95G>T
ENST00000677407.1:c.669+137G>T	ENSP00000503141.1:n.669+137G>T
ENST00000677490.1:c.669+137G>T	ENSP00000503255.1:n.669+137G>T
ENST00000677567.1:c.669+137G>T	ENSP00000503217.1:n.669+137G>T
ENST00000677692.1:n.902G>T
ENST00000677764.1:c.669+137G>T	ENSP00000504547.1:n.669+137G>T
ENST00000677979.1:c.*148+137G>T	ENSP00000503341.1:n.*148+137G>T
ENST00000678158.1:c.669+137G>T	ENSP00000504765.1:n.669+137G>T
ENST00000678188.1:n.985G>T
ENST00000678289.1:c.669+137G>T	ENSP00000504063.1:n.669+137G>T
ENST00000678455.1:c.666+137G>T	ENSP00000504395.1:n.666+137G>T
ENST00000678468.1:c.*2+93G>T	ENSP00000503925.1:n.*2+93G>T
ENST00000678562.1:c.*599G>T	ENSP00000502954.1:n.*599G>T
ENST00000678737.1:c.669+137G>T	ENSP00000503770.1:n.669+137G>T
ENST00000678832.1:c.*325+137G>T	ENSP00000502992.1:n.*325+137G>T
ENST00000678898.1:n.902G>T
ENST00000678914.1:c.567+239G>T	ENSP00000504515.1:n.567+239G>T
ENST00000679158.1:c.669+137G>T	ENSP00000503837.1:n.669+137G>T
ENST00000679183.1:c.669+137G>T	ENSP00000503016.1:n.669+137G>T
ENST00000679308.1:c.669+137G>T	ENSP00000503148.1:n.669+137G>T
ENST00000679332.1:n.902G>T
ENST00000252711.6:c.669+137G>T	ENSP00000252711.2:n.669+137G>T
ENST00000307300.8:c.759+167G>T	ENSP00000302321.4:n.759+167G>T
ENST00000404554.5:c.669+137G>T	ENSP00000385697.1:n.669+137G>T
ENST00000443626.5:c.547+3951G>T	ENSP00000411527.1:n.547+3951G>T
ENST00000485344.6:n.828G>T
ENST00000620965.4:c.669+137G>T	ENSP00000480897.1:n.669+137G>T
NM_004544.3:c.669+137G>T	NP_004535.1:n.669+137G>T
XM_006712543.1:c.669+137G>T	XP_006712606.1:n.669+137G>T
XM_011511228.1:c.669+137G>T	XP_011509530.1:n.669+137G>T
XM_011511229.1:c.669+137G>T	XP_011509531.1:n.669+137G>T
NM_001322019.1:c.669+137G>T	NP_001308948.1:n.669+137G>T
NM_001322020.1:c.669+137G>T	NP_001308949.1:n.669+137G>T
NR_136155.1:n.907G>T
NR_136156.1:n.907G>T
NR_136157.1:n.738G>T
NR_136158.1:n.907G>T
XM_011511228.3:c.669+137G>T	XP_011509530.1:n.669+137G>T
XR_001738750.2:n.711+137G>T
NM_004544.4:c.669+137G>T MANE Select	NP_004535.1:n.669+137G>T
NM_001322020.2:c.669+137G>T	NP_001308949.1:n.669+137G>T
NR_136155.2:n.847G>T
NR_136156.2:n.847G>T
NR_136157.2:n.678G>T
NR_136158.2:n.847G>T
NM_001322019.2:c.669+137G>T	NP_001308948.1:n.669+137G>T