Canonical Allele Identifier: CA10614723

Gene: NDUFA10

Linked Data

• ClinVar Variation Id: 335196
• ClinVar RCV Id: RCV000267063 ; RCV000361689
• dbSNP Id: rs539829771
• gnomAD v2: 2-240900146-G-A
• gnomAD v3: 2-239960729-G-A
• gnomAD v4: 2-239960729-G-A
• MyVariant Identifiers: chr2:g.240900146G>A (hg19) ; chr2:g.239960729G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.239960729G>A , CM000664.2:g.239960729G>A	GRCh38
NC_000002.11:g.240900146G>A , CM000664.1:g.240900146G>A	GRCh37
NC_000002.10:g.240548819G>A	NCBI36
NG_031855.1:g.69674C>T
NG_031855.2:g.69674C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000252711.7:c.*389C>T MANE Select	ENSP00000252711.2:n.*389C>T
ENST00000476216.6:n.4596C>T
ENST00000676491.1:c.1000-1692C>T	ENSP00000504528.1:n.1000-1692C>T
ENST00000676782.1:c.1000-22019C>T	ENSP00000504717.1:n.1000-22019C>T
ENST00000676929.1:c.*95+294C>T	ENSP00000503956.1:n.*95+294C>T
ENST00000677057.1:n.4028+44481C>T
ENST00000677155.1:c.*646C>T	ENSP00000502921.1:n.*646C>T
ENST00000677294.1:c.*389C>T	ENSP00000503461.1:n.*389C>T
ENST00000677324.1:n.3954C>T
ENST00000677395.1:c.*3153C>T	ENSP00000502890.1:n.*3153C>T
ENST00000677407.1:c.1000-9711C>T	ENSP00000503141.1:n.1000-9711C>T
ENST00000677692.1:n.4260+226C>T
ENST00000677764.1:c.*768C>T	ENSP00000504547.1:n.*768C>T
ENST00000677979.1:c.*936C>T	ENSP00000503341.1:n.*936C>T
ENST00000678158.1:c.*163+226C>T	ENSP00000504765.1:n.*163+226C>T
ENST00000678188.1:n.4678C>T
ENST00000678455.1:c.*389C>T	ENSP00000504395.1:n.*389C>T
ENST00000678468.1:c.*995C>T	ENSP00000503925.1:n.*995C>T
ENST00000678562.1:c.*4292C>T	ENSP00000502954.1:n.*4292C>T
ENST00000678832.1:c.*1113C>T	ENSP00000502992.1:n.*1113C>T
ENST00000678914.1:c.*389C>T	ENSP00000504515.1:n.*389C>T
ENST00000679183.1:c.999+29345C>T	ENSP00000503016.1:n.999+29345C>T
ENST00000252711.6:c.*389C>T	ENSP00000252711.2:n.*389C>T
ENST00000419408.5:c.294+29345C>T	ENSP00000408055.1:n.294+29345C>T
ENST00000471378.1:n.82-1692C>T
NM_004544.3:c.*389C>T	NP_004535.1:n.*389C>T
XM_011511229.1:c.*394C>T	XP_011509531.1:n.*394C>T
NM_001322020.1:c.*394C>T	NP_001308949.1:n.*394C>T
NR_136155.1:n.4600C>T
NR_136156.1:n.4491C>T
NR_136157.1:n.4431C>T
NR_136158.1:n.4033+44481C>T
XR_001738750.2:n.1704C>T
NM_004544.4:c.*389C>T MANE Select	NP_004535.1:n.*389C>T
NM_001322020.2:c.*394C>T	NP_001308949.1:n.*394C>T
NR_136155.2:n.4540C>T
NR_136156.2:n.4431C>T
NR_136157.2:n.4371C>T
NR_136158.2:n.3973+44481C>T