Canonical Allele Identifier: CA2607657495

Gene: NDUFA10

Linked Data

• gnomAD v3: 2-240014717-C-CTTTGATTGAAAACTGCATTACA
• gnomAD v4: 2-240014717-C-CTTTGATTGAAAACTGCATTACA

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.240014719_240014740dup , CM000664.2:g.240014719_240014740dup	GRCh38
NC_000002.11:g.240954136_240954157dup , CM000664.1:g.240954136_240954157dup	GRCh37
NC_000002.10:g.240602809_240602830dup	NCBI36
NG_031855.1:g.15664_15685dup
NG_031855.2:g.15664_15685dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000252711.7:c.669_669+21dup
ENST00000414580.2:c.*215_*236dup	ENSP00000388413.2:n.*215_*236dup
ENST00000444548.6:c.669_669+21dup
ENST00000448880.6:c.669_669+21dup
ENST00000476216.6:n.766_787dup
ENST00000620965.5:c.669_669+21dup
ENST00000676491.1:c.669_669+21dup
ENST00000676782.1:c.669_669+21dup
ENST00000676784.1:n.755_776dup
ENST00000676929.1:c.669_669+21dup
ENST00000677057.1:n.765_786dup
ENST00000677114.1:c.547+3814_547+3835dup	ENSP00000504818.1:n.547+3814_547+3835dup
ENST00000677155.1:c.547+3814_547+3835dup	ENSP00000502921.1:n.547+3814_547+3835dup
ENST00000677263.1:c.669_669+21dup
ENST00000677294.1:c.639+30_639+51dup	ENSP00000503461.1:n.639+30_639+51dup
ENST00000677368.1:c.547+3814_547+3835dup	ENSP00000502983.1:n.547+3814_547+3835dup
ENST00000677395.1:c.669_690dup	ENSP00000502890.1:p.Gly231CysfsTer20
ENST00000677407.1:c.669_669+21dup
ENST00000677490.1:c.669_669+21dup
ENST00000677567.1:c.669_669+21dup
ENST00000677692.1:n.765_786dup
ENST00000677764.1:c.669_669+21dup
ENST00000677979.1:c.*148_*148+21dup
ENST00000678158.1:c.669_669+21dup
ENST00000678188.1:n.848_869dup
ENST00000678289.1:c.669_669+21dup
ENST00000678455.1:c.666_666+21dup
ENST00000678468.1:c.669_690dup	ENSP00000503925.1:p.Gly231CysfsTer?
ENST00000678562.1:c.*462_*483dup	ENSP00000502954.1:n.*462_*483dup
ENST00000678737.1:c.669_669+21dup
ENST00000678832.1:c.*325_*325+21dup
ENST00000678898.1:n.765_786dup
ENST00000678914.1:c.567+102_567+123dup	ENSP00000504515.1:n.567+102_567+123dup
ENST00000679158.1:c.669_669+21dup
ENST00000679183.1:c.669_669+21dup
ENST00000679308.1:c.669_669+21dup
ENST00000679332.1:n.765_786dup
ENST00000252711.6:c.669_669+21dup
ENST00000307300.8:c.759+30_759+51dup	ENSP00000302321.4:n.759+30_759+51dup
ENST00000404554.5:c.669_669+21dup
ENST00000443626.5:c.547+3814_547+3835dup	ENSP00000411527.1:n.547+3814_547+3835dup
ENST00000485344.6:n.691_712dup
ENST00000620965.4:c.669_669+21dup
NM_004544.3:c.669_669+21dup
XM_006712543.1:c.669_669+21dup
XM_011511228.1:c.669_669+21dup
XM_011511229.1:c.669_669+21dup
NM_001322019.1:c.669_669+21dup
NM_001322020.1:c.669_669+21dup
NR_136155.1:n.770_791dup
NR_136156.1:n.770_791dup
NR_136157.1:n.601_622dup
NR_136158.1:n.770_791dup
XM_011511228.3:c.669_669+21dup
XR_001738750.2:n.711_711+21dup
NM_004544.4:c.669_669+21dup
NM_001322020.2:c.669_669+21dup
NR_136155.2:n.710_731dup
NR_136156.2:n.710_731dup
NR_136157.2:n.541_562dup
NR_136158.2:n.710_731dup
NM_001322019.2:c.669_669+21dup