Canonical Allele Identifier: CA10614936

Gene: NDUFA10

Linked Data

• ClinVar Variation Id: 335173
• ClinVar RCV Id: RCV000340471 ; RCV000405302
• dbSNP Id: rs886055818
• MyVariant Identifiers: chr2:g.240898493T>G (hg19) ; chr2:g.239959076T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.239959076T>G , CM000664.2:g.239959076T>G	GRCh38
NC_000002.11:g.240898493T>G , CM000664.1:g.240898493T>G	GRCh37
NC_000002.10:g.240547166T>G	NCBI36
NG_031855.1:g.71327A>C
NG_031855.2:g.71327A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252711.7:c.*2042A>C MANE Select	ENSP00000252711.2:n.*2042A>C
ENST00000476216.6:n.6249A>C
ENST00000676491.1:c.1000-39A>C	ENSP00000504528.1:n.1000-39A>C
ENST00000676782.1:c.1000-20366A>C	ENSP00000504717.1:n.1000-20366A>C
ENST00000676929.1:c.*96-39A>C	ENSP00000503956.1:n.*96-39A>C
ENST00000677057.1:n.4029-46086A>C
ENST00000677155.1:c.*2299A>C	ENSP00000502921.1:n.*2299A>C
ENST00000677294.1:c.*2042A>C	ENSP00000503461.1:n.*2042A>C
ENST00000677324.1:n.5607A>C
ENST00000677395.1:c.*4806A>C	ENSP00000502890.1:n.*4806A>C
ENST00000677407.1:c.1000-8058A>C	ENSP00000503141.1:n.1000-8058A>C
ENST00000677692.1:n.4261-39A>C
ENST00000677764.1:c.*2421A>C	ENSP00000504547.1:n.*2421A>C
ENST00000677979.1:c.*2589A>C	ENSP00000503341.1:n.*2589A>C
ENST00000678158.1:c.*164-39A>C	ENSP00000504765.1:n.*164-39A>C
ENST00000678188.1:n.6331A>C
ENST00000678455.1:c.*2042A>C	ENSP00000504395.1:n.*2042A>C
ENST00000678468.1:c.*2648A>C	ENSP00000503925.1:n.*2648A>C
ENST00000678562.1:c.*5945A>C	ENSP00000502954.1:n.*5945A>C
ENST00000678832.1:c.*2766A>C	ENSP00000502992.1:n.*2766A>C
ENST00000678914.1:c.*2042A>C	ENSP00000504515.1:n.*2042A>C
ENST00000679183.1:c.999+30998A>C	ENSP00000503016.1:n.999+30998A>C
ENST00000252711.6:c.*2042A>C	ENSP00000252711.2:n.*2042A>C
ENST00000419408.5:c.294+30998A>C	ENSP00000408055.1:n.294+30998A>C
ENST00000471378.1:n.82-39A>C
NM_004544.3:c.*2042A>C	NP_004535.1:n.*2042A>C
NM_001322020.1:c.*2047A>C	NP_001308949.1:n.*2047A>C
NR_136155.1:n.6253A>C
NR_136156.1:n.6144A>C
NR_136157.1:n.6084A>C
NR_136158.1:n.4034-46086A>C
NM_004544.4:c.*2042A>C MANE Select	NP_004535.1:n.*2042A>C
NM_001322020.2:c.*2047A>C	NP_001308949.1:n.*2047A>C
NR_136155.2:n.6193A>C
NR_136156.2:n.6084A>C
NR_136157.2:n.6024A>C
NR_136158.2:n.3974-46086A>C