Canonical Allele Identifier: CA351272800

Gene: NDUFA10

Linked Data

• MyVariant Identifiers: chr2:g.240954191G>A (hg19) ; chr2:g.240014774G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.240014774G>A , CM000664.2:g.240014774G>A	GRCh38
NC_000002.11:g.240954191G>A , CM000664.1:g.240954191G>A	GRCh37
NC_000002.10:g.240602864G>A	NCBI36
NG_031855.1:g.15629C>T
NG_031855.2:g.15629C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252711.7:c.634C>T MANE Select	ENSP00000252711.2:p.Pro212Ser
ENST00000414580.2:c.*180C>T	ENSP00000388413.2:n.*180C>T
ENST00000444548.6:c.634C>T	ENSP00000403080.2:p.Pro212Ser
ENST00000448880.6:c.634C>T	ENSP00000408224.2:p.Pro212Ser
ENST00000476216.6:n.731C>T
ENST00000620965.5:c.634C>T	ENSP00000480897.2:p.Pro212Ser
ENST00000676491.1:c.634C>T	ENSP00000504528.1:p.Pro212Ser
ENST00000676782.1:c.634C>T	ENSP00000504717.1:p.Pro212Ser
ENST00000676784.1:n.720C>T
ENST00000676929.1:c.634C>T	ENSP00000503956.1:p.Pro212Ser
ENST00000677057.1:n.730C>T
ENST00000677114.1:c.547+3779C>T	ENSP00000504818.1:n.547+3779C>T
ENST00000677155.1:c.547+3779C>T	ENSP00000502921.1:n.547+3779C>T
ENST00000677263.1:c.634C>T	ENSP00000503790.1:p.Pro212Ser
ENST00000677294.1:c.634C>T	ENSP00000503461.1:p.Pro212Ser
ENST00000677368.1:c.547+3779C>T	ENSP00000502983.1:n.547+3779C>T
ENST00000677395.1:c.634C>T	ENSP00000502890.1:p.Pro212Ser
ENST00000677407.1:c.634C>T	ENSP00000503141.1:p.Pro212Ser
ENST00000677490.1:c.634C>T	ENSP00000503255.1:p.Pro212Ser
ENST00000677567.1:c.634C>T	ENSP00000503217.1:p.Pro212Ser
ENST00000677692.1:n.730C>T
ENST00000677764.1:c.634C>T	ENSP00000504547.1:p.Pro212Ser
ENST00000677979.1:c.*113C>T	ENSP00000503341.1:n.*113C>T
ENST00000678158.1:c.634C>T	ENSP00000504765.1:p.Pro212Ser
ENST00000678188.1:n.813C>T
ENST00000678289.1:c.634C>T	ENSP00000504063.1:p.Pro212Ser
ENST00000678455.1:c.631C>T	ENSP00000504395.1:p.Pro211Ser
ENST00000678468.1:c.634C>T	ENSP00000503925.1:p.Pro212Ser
ENST00000678562.1:c.*427C>T	ENSP00000502954.1:n.*427C>T
ENST00000678737.1:c.634C>T	ENSP00000503770.1:p.Pro212Ser
ENST00000678832.1:c.*290C>T	ENSP00000502992.1:n.*290C>T
ENST00000678898.1:n.730C>T
ENST00000678914.1:c.567+67C>T	ENSP00000504515.1:n.567+67C>T
ENST00000679158.1:c.634C>T	ENSP00000503837.1:p.Pro212Ser
ENST00000679183.1:c.634C>T	ENSP00000503016.1:p.Pro212Ser
ENST00000679308.1:c.634C>T	ENSP00000503148.1:p.Pro212Ser
ENST00000679332.1:n.730C>T
ENST00000252711.6:c.634C>T	ENSP00000252711.2:p.Pro212Ser
ENST00000307300.8:c.754C>T	ENSP00000302321.4:p.Pro252Ser
ENST00000404554.5:c.634C>T	ENSP00000385697.1:p.Pro212Ser
ENST00000443626.5:c.547+3779C>T	ENSP00000411527.1:n.547+3779C>T
ENST00000485344.6:n.656C>T
ENST00000620965.4:c.634C>T	ENSP00000480897.1:p.Pro212Ser
NM_004544.3:c.634C>T	NP_004535.1:p.Pro212Ser
XM_006712543.1:c.634C>T	XP_006712606.1:p.Pro212Ser
XM_011511228.1:c.634C>T	XP_011509530.1:p.Pro212Ser
XM_011511229.1:c.634C>T	XP_011509531.1:p.Pro212Ser
NM_001322019.1:c.634C>T	NP_001308948.1:p.Pro212Ser
NM_001322020.1:c.634C>T	NP_001308949.1:p.Pro212Ser
NR_136155.1:n.735C>T
NR_136156.1:n.735C>T
NR_136157.1:n.566C>T
NR_136158.1:n.735C>T
XM_011511228.3:c.634C>T	XP_011509530.1:p.Pro212Ser
XR_001738750.2:n.676C>T
NM_004544.4:c.634C>T MANE Select	NP_004535.1:p.Pro212Ser
NM_001322020.2:c.634C>T	NP_001308949.1:p.Pro212Ser
NR_136155.2:n.675C>T
NR_136156.2:n.675C>T
NR_136157.2:n.506C>T
NR_136158.2:n.675C>T
NM_001322019.2:c.634C>T	NP_001308948.1:p.Pro212Ser