Canonical Allele Identifier: CA10614955

Gene: NDUFA10

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.239960704C>T , CM000664.2:g.239960704C>T	GRCh38
NC_000002.11:g.240900121C>T , CM000664.1:g.240900121C>T	GRCh37
NC_000002.10:g.240548794C>T	NCBI36
NG_031855.1:g.69699G>A
NG_031855.2:g.69699G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252711.7:c.*414G>A MANE Select	ENSP00000252711.2:n.*414G>A
ENST00000476216.6:n.4621G>A
ENST00000676491.1:c.1000-1667G>A	ENSP00000504528.1:n.1000-1667G>A
ENST00000676782.1:c.1000-21994G>A	ENSP00000504717.1:n.1000-21994G>A
ENST00000676929.1:c.*95+319G>A	ENSP00000503956.1:n.*95+319G>A
ENST00000677057.1:n.4028+44506G>A
ENST00000677155.1:c.*671G>A	ENSP00000502921.1:n.*671G>A
ENST00000677294.1:c.*414G>A	ENSP00000503461.1:n.*414G>A
ENST00000677324.1:n.3979G>A
ENST00000677395.1:c.*3178G>A	ENSP00000502890.1:n.*3178G>A
ENST00000677407.1:c.1000-9686G>A	ENSP00000503141.1:n.1000-9686G>A
ENST00000677692.1:n.4260+251G>A
ENST00000677764.1:c.*793G>A	ENSP00000504547.1:n.*793G>A
ENST00000677979.1:c.*961G>A	ENSP00000503341.1:n.*961G>A
ENST00000678158.1:c.*163+251G>A	ENSP00000504765.1:n.*163+251G>A
ENST00000678188.1:n.4703G>A
ENST00000678455.1:c.*414G>A	ENSP00000504395.1:n.*414G>A
ENST00000678468.1:c.*1020G>A	ENSP00000503925.1:n.*1020G>A
ENST00000678562.1:c.*4317G>A	ENSP00000502954.1:n.*4317G>A
ENST00000678832.1:c.*1138G>A	ENSP00000502992.1:n.*1138G>A
ENST00000678914.1:c.*414G>A	ENSP00000504515.1:n.*414G>A
ENST00000679183.1:c.999+29370G>A	ENSP00000503016.1:n.999+29370G>A
ENST00000252711.6:c.*414G>A	ENSP00000252711.2:n.*414G>A
ENST00000419408.5:c.294+29370G>A	ENSP00000408055.1:n.294+29370G>A
ENST00000471378.1:n.82-1667G>A
NM_004544.3:c.*414G>A	NP_004535.1:n.*414G>A
XM_011511229.1:c.*419G>A	XP_011509531.1:n.*419G>A
NM_001322020.1:c.*419G>A	NP_001308949.1:n.*419G>A
NR_136155.1:n.4625G>A
NR_136156.1:n.4516G>A
NR_136157.1:n.4456G>A
NR_136158.1:n.4033+44506G>A
NM_004544.4:c.*414G>A MANE Select	NP_004535.1:n.*414G>A
NM_001322020.2:c.*419G>A	NP_001308949.1:n.*419G>A
NR_136155.2:n.4565G>A
NR_136156.2:n.4456G>A
NR_136157.2:n.4396G>A
NR_136158.2:n.3973+44506G>A