Canonical Allele Identifier: CA2663931237

Gene: NDUFA10

Linked Data

• gnomAD v4: 2-240014698-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.240014698C>G , CM000664.2:g.240014698C>G	GRCh38
NC_000002.11:g.240954115C>G , CM000664.1:g.240954115C>G	GRCh37
NC_000002.10:g.240602788C>G	NCBI36
NG_031855.1:g.15705G>C
NG_031855.2:g.15705G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000252711.7:c.669+41G>C MANE Select	ENSP00000252711.2:n.669+41G>C
ENST00000414580.2:c.*256G>C	ENSP00000388413.2:n.*256G>C
ENST00000444548.6:c.669+41G>C	ENSP00000403080.2:n.669+41G>C
ENST00000448880.6:c.669+41G>C	ENSP00000408224.2:n.669+41G>C
ENST00000476216.6:n.807G>C
ENST00000620965.5:c.669+41G>C	ENSP00000480897.2:n.669+41G>C
ENST00000676491.1:c.669+41G>C	ENSP00000504528.1:n.669+41G>C
ENST00000676782.1:c.669+41G>C	ENSP00000504717.1:n.669+41G>C
ENST00000676784.1:n.796G>C
ENST00000676929.1:c.669+41G>C	ENSP00000503956.1:n.669+41G>C
ENST00000677057.1:n.806G>C
ENST00000677114.1:c.547+3855G>C	ENSP00000504818.1:n.547+3855G>C
ENST00000677155.1:c.547+3855G>C	ENSP00000502921.1:n.547+3855G>C
ENST00000677263.1:c.669+41G>C	ENSP00000503790.1:n.669+41G>C
ENST00000677294.1:c.639+71G>C	ENSP00000503461.1:n.639+71G>C
ENST00000677368.1:c.547+3855G>C	ENSP00000502983.1:n.547+3855G>C
ENST00000677395.1:c.710G>C	ENSP00000502890.1:p.Ter237Ser
ENST00000677407.1:c.669+41G>C	ENSP00000503141.1:n.669+41G>C
ENST00000677490.1:c.669+41G>C	ENSP00000503255.1:n.669+41G>C
ENST00000677567.1:c.669+41G>C	ENSP00000503217.1:n.669+41G>C
ENST00000677692.1:n.806G>C
ENST00000677764.1:c.669+41G>C	ENSP00000504547.1:n.669+41G>C
ENST00000677979.1:c.*148+41G>C	ENSP00000503341.1:n.*148+41G>C
ENST00000678158.1:c.669+41G>C	ENSP00000504765.1:n.669+41G>C
ENST00000678188.1:n.889G>C
ENST00000678289.1:c.669+41G>C	ENSP00000504063.1:n.669+41G>C
ENST00000678455.1:c.666+41G>C	ENSP00000504395.1:n.666+41G>C
ENST00000678468.1:c.710G>C	ENSP00000503925.1:p.Ter237Ser
ENST00000678562.1:c.*503G>C	ENSP00000502954.1:n.*503G>C
ENST00000678737.1:c.669+41G>C	ENSP00000503770.1:n.669+41G>C
ENST00000678832.1:c.*325+41G>C	ENSP00000502992.1:n.*325+41G>C
ENST00000678898.1:n.806G>C
ENST00000678914.1:c.567+143G>C	ENSP00000504515.1:n.567+143G>C
ENST00000679158.1:c.669+41G>C	ENSP00000503837.1:n.669+41G>C
ENST00000679183.1:c.669+41G>C	ENSP00000503016.1:n.669+41G>C
ENST00000679308.1:c.669+41G>C	ENSP00000503148.1:n.669+41G>C
ENST00000679332.1:n.806G>C
ENST00000252711.6:c.669+41G>C	ENSP00000252711.2:n.669+41G>C
ENST00000307300.8:c.759+71G>C	ENSP00000302321.4:n.759+71G>C
ENST00000404554.5:c.669+41G>C	ENSP00000385697.1:n.669+41G>C
ENST00000443626.5:c.547+3855G>C	ENSP00000411527.1:n.547+3855G>C
ENST00000485344.6:n.732G>C
ENST00000620965.4:c.669+41G>C	ENSP00000480897.1:n.669+41G>C
NM_004544.3:c.669+41G>C	NP_004535.1:n.669+41G>C
XM_006712543.1:c.669+41G>C	XP_006712606.1:n.669+41G>C
XM_011511228.1:c.669+41G>C	XP_011509530.1:n.669+41G>C
XM_011511229.1:c.669+41G>C	XP_011509531.1:n.669+41G>C
NM_001322019.1:c.669+41G>C	NP_001308948.1:n.669+41G>C
NM_001322020.1:c.669+41G>C	NP_001308949.1:n.669+41G>C
NR_136155.1:n.811G>C
NR_136156.1:n.811G>C
NR_136157.1:n.642G>C
NR_136158.1:n.811G>C
XM_011511228.3:c.669+41G>C	XP_011509530.1:n.669+41G>C
XR_001738750.2:n.711+41G>C
NM_004544.4:c.669+41G>C MANE Select	NP_004535.1:n.669+41G>C
NM_001322020.2:c.669+41G>C	NP_001308949.1:n.669+41G>C
NR_136155.2:n.751G>C
NR_136156.2:n.751G>C
NR_136157.2:n.582G>C
NR_136158.2:n.751G>C
NM_001322019.2:c.669+41G>C	NP_001308948.1:n.669+41G>C