Canonical Allele Identifier: CA68048980

Gene: NDUFA10

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.239960935G>A , CM000664.2:g.239960935G>A	GRCh38
NC_000002.11:g.240900352G>A , CM000664.1:g.240900352G>A	GRCh37
NC_000002.10:g.240549025G>A	NCBI36
NG_031855.1:g.69468C>T
NG_031855.2:g.69468C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_004544.4:c.*183C>T MANE Select	NP_004535.1:n.*183C>T
ENST00000252711.7:c.*183C>T MANE Select	ENSP00000252711.2:n.*183C>T
NM_001322020.1:c.*188C>T	NP_001308949.1:n.*188C>T
NM_001322020.2:c.*188C>T	NP_001308949.1:n.*188C>T
NM_004544.3:c.*183C>T	NP_004535.1:n.*183C>T
NR_136155.1:n.4394C>T
NR_136155.2:n.4334C>T
NR_136156.1:n.4285C>T
NR_136156.2:n.4225C>T
NR_136157.1:n.4225C>T
NR_136157.2:n.4165C>T
NR_136158.1:n.4033+44275C>T
NR_136158.2:n.3973+44275C>T
ENST00000252711.6:c.*183C>T	ENSP00000252711.2:n.*183C>T
ENST00000404554.5:c.*183C>T	ENSP00000385697.1:n.*183C>T
ENST00000419408.5:c.294+29139C>T	ENSP00000408055.1:n.294+29139C>T
ENST00000471378.1:n.82-1898C>T
ENST00000476216.5:n.613C>T
ENST00000476216.6:n.4390C>T
ENST00000485344.6:n.4315C>T
ENST00000620965.4:c.*183C>T	ENSP00000480897.1:n.*183C>T
ENST00000620965.5:c.*183C>T	ENSP00000480897.2:n.*183C>T
ENST00000676491.1:c.1000-1898C>T	ENSP00000504528.1:n.1000-1898C>T
ENST00000676782.1:c.1000-22225C>T	ENSP00000504717.1:n.1000-22225C>T
ENST00000676929.1:c.*95+88C>T	ENSP00000503956.1:n.*95+88C>T
ENST00000677057.1:n.4028+44275C>T
ENST00000677114.1:c.*645C>T	ENSP00000504818.1:n.*645C>T
ENST00000677155.1:c.*440C>T	ENSP00000502921.1:n.*440C>T
ENST00000677294.1:c.*183C>T	ENSP00000503461.1:n.*183C>T
ENST00000677324.1:n.3748C>T
ENST00000677395.1:c.*2947C>T	ENSP00000502890.1:n.*2947C>T
ENST00000677407.1:c.1000-9917C>T	ENSP00000503141.1:n.1000-9917C>T
ENST00000677567.1:c.*148C>T	ENSP00000503217.1:n.*148C>T
ENST00000677692.1:n.4260+20C>T
ENST00000677764.1:c.*562C>T	ENSP00000504547.1:n.*562C>T
ENST00000677979.1:c.*730C>T	ENSP00000503341.1:n.*730C>T
ENST00000678158.1:c.*163+20C>T	ENSP00000504765.1:n.*163+20C>T
ENST00000678188.1:n.4472C>T
ENST00000678455.1:c.*183C>T	ENSP00000504395.1:n.*183C>T
ENST00000678468.1:c.*789C>T	ENSP00000503925.1:n.*789C>T
ENST00000678562.1:c.*4086C>T	ENSP00000502954.1:n.*4086C>T
ENST00000678832.1:c.*907C>T	ENSP00000502992.1:n.*907C>T
ENST00000678914.1:c.*183C>T	ENSP00000504515.1:n.*183C>T
ENST00000679158.1:c.*188C>T	ENSP00000503837.1:n.*188C>T
ENST00000679183.1:c.999+29139C>T	ENSP00000503016.1:n.999+29139C>T
ENST00000679308.1:c.*306C>T	ENSP00000503148.1:n.*306C>T
XM_011511229.1:c.*188C>T	XP_011509531.1:n.*188C>T
XR_001738750.2:n.1498C>T