Canonical Allele Identifier: CA10614906

Gene: NDUFA10

Linked Data

• ClinVar Variation Id: 335162
• ClinVar RCV Id: RCV000310655 ; RCV000408151
• dbSNP Id: rs886055814
• MyVariant Identifiers: chr2:g.240897538C>T (hg19) ; chr2:g.239958121C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.239958121C>T , CM000664.2:g.239958121C>T	GRCh38
NC_000002.11:g.240897538C>T , CM000664.1:g.240897538C>T	GRCh37
NC_000002.10:g.240546211C>T	NCBI36
NG_031855.1:g.72282G>A
NG_031855.2:g.72282G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252711.7:c.*2997G>A MANE Select	ENSP00000252711.2:n.*2997G>A
ENST00000476216.6:n.7204G>A
ENST00000676491.1:c.*830G>A	ENSP00000504528.1:n.*830G>A
ENST00000676782.1:c.1000-19411G>A	ENSP00000504717.1:n.1000-19411G>A
ENST00000676929.1:c.*1012G>A	ENSP00000503956.1:n.*1012G>A
ENST00000677057.1:n.4029-45131G>A
ENST00000677155.1:c.*3254G>A	ENSP00000502921.1:n.*3254G>A
ENST00000677294.1:c.*2997G>A	ENSP00000503461.1:n.*2997G>A
ENST00000677324.1:n.6562G>A
ENST00000677395.1:c.*5761G>A	ENSP00000502890.1:n.*5761G>A
ENST00000677407.1:c.1000-7103G>A	ENSP00000503141.1:n.1000-7103G>A
ENST00000677692.1:n.5177G>A
ENST00000677764.1:c.*3376G>A	ENSP00000504547.1:n.*3376G>A
ENST00000677979.1:c.*3544G>A	ENSP00000503341.1:n.*3544G>A
ENST00000678158.1:c.*1080G>A	ENSP00000504765.1:n.*1080G>A
ENST00000678188.1:n.7286G>A
ENST00000678455.1:c.*2997G>A	ENSP00000504395.1:n.*2997G>A
ENST00000678468.1:c.*3603G>A	ENSP00000503925.1:n.*3603G>A
ENST00000678562.1:c.*6900G>A	ENSP00000502954.1:n.*6900G>A
ENST00000678832.1:c.*3721G>A	ENSP00000502992.1:n.*3721G>A
ENST00000678914.1:c.*2997G>A	ENSP00000504515.1:n.*2997G>A
ENST00000679183.1:c.999+31953G>A	ENSP00000503016.1:n.999+31953G>A
ENST00000252711.6:c.*2997G>A	ENSP00000252711.2:n.*2997G>A
ENST00000419408.5:c.294+31953G>A	ENSP00000408055.1:n.294+31953G>A
NM_004544.3:c.*2997G>A	NP_004535.1:n.*2997G>A
NM_001322020.1:c.*3002G>A	NP_001308949.1:n.*3002G>A
NR_136155.1:n.7208G>A
NR_136156.1:n.7099G>A
NR_136157.1:n.7039G>A
NR_136158.1:n.4034-45131G>A
NM_004544.4:c.*2997G>A MANE Select	NP_004535.1:n.*2997G>A
NM_001322020.2:c.*3002G>A	NP_001308949.1:n.*3002G>A
NR_136155.2:n.7148G>A
NR_136156.2:n.7039G>A
NR_136157.2:n.6979G>A
NR_136158.2:n.3974-45131G>A