Canonical Allele Identifier: CA351276136

Gene: NDUFA10

Linked Data

• MyVariant Identifiers: chr2:g.240900552A>T (hg19) ; chr2:g.239961135A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.239961135A>T , CM000664.2:g.239961135A>T	GRCh38
NC_000002.11:g.240900552A>T , CM000664.1:g.240900552A>T	GRCh37
NC_000002.10:g.240549225A>T	NCBI36
NG_031855.1:g.69268T>A
NG_031855.2:g.69268T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252711.7:c.1051T>A MANE Select	ENSP00000252711.2:p.Trp351Arg
ENST00000476216.6:n.4190T>A
ENST00000620965.5:c.1099T>A	ENSP00000480897.2:p.Trp367Arg
ENST00000676491.1:c.1000-2098T>A	ENSP00000504528.1:n.1000-2098T>A
ENST00000676782.1:c.1000-22425T>A	ENSP00000504717.1:n.1000-22425T>A
ENST00000676929.1:c.1051T>A	ENSP00000503956.1:p.Trp351Arg
ENST00000677057.1:n.4028+44075T>A
ENST00000677114.1:c.*445T>A	ENSP00000504818.1:n.*445T>A
ENST00000677155.1:c.*240T>A	ENSP00000502921.1:n.*240T>A
ENST00000677294.1:c.877T>A	ENSP00000503461.1:p.Trp293Arg
ENST00000677324.1:n.3548T>A
ENST00000677395.1:c.*2747T>A	ENSP00000502890.1:n.*2747T>A
ENST00000677407.1:c.1000-10117T>A	ENSP00000503141.1:n.1000-10117T>A
ENST00000677567.1:c.1130T>A	ENSP00000503217.1:p.Val377Glu
ENST00000677692.1:n.4080T>A
ENST00000677764.1:c.*362T>A	ENSP00000504547.1:n.*362T>A
ENST00000677979.1:c.*530T>A	ENSP00000503341.1:n.*530T>A
ENST00000678158.1:c.1051T>A	ENSP00000504765.1:p.Trp351Arg
ENST00000678188.1:n.4272T>A
ENST00000678455.1:c.1048T>A	ENSP00000504395.1:p.Trp350Arg
ENST00000678468.1:c.*589T>A	ENSP00000503925.1:n.*589T>A
ENST00000678562.1:c.*3886T>A	ENSP00000502954.1:n.*3886T>A
ENST00000678832.1:c.*707T>A	ENSP00000502992.1:n.*707T>A
ENST00000678914.1:c.949T>A	ENSP00000504515.1:p.Trp317Arg
ENST00000679158.1:c.942T>A	ENSP00000503837.1:p.Ser314Arg
ENST00000679183.1:c.999+28939T>A	ENSP00000503016.1:n.999+28939T>A
ENST00000679308.1:c.*106T>A	ENSP00000503148.1:n.*106T>A
ENST00000252711.6:c.1051T>A	ENSP00000252711.2:p.Trp351Arg
ENST00000404554.5:c.1156T>A	ENSP00000385697.1:p.Trp386Arg
ENST00000419408.5:c.294+28939T>A	ENSP00000408055.1:n.294+28939T>A
ENST00000471378.1:n.82-2098T>A
ENST00000476216.5:n.413T>A
ENST00000485344.6:n.4115T>A
ENST00000620965.4:c.1051T>A	ENSP00000480897.1:p.Trp351Arg
NM_004544.3:c.1051T>A	NP_004535.1:p.Trp351Arg
XM_011511229.1:c.942T>A	XP_011509531.1:p.Ser314Arg
NM_001322020.1:c.942T>A	NP_001308949.1:p.Ser314Arg
NR_136155.1:n.4194T>A
NR_136156.1:n.4085T>A
NR_136157.1:n.4025T>A
NR_136158.1:n.4033+44075T>A
XR_001738750.2:n.1298T>A
NM_004544.4:c.1051T>A MANE Select	NP_004535.1:p.Trp351Arg
NM_001322020.2:c.942T>A	NP_001308949.1:p.Ser314Arg
NR_136155.2:n.4134T>A
NR_136156.2:n.4025T>A
NR_136157.2:n.3965T>A
NR_136158.2:n.3973+44075T>A