Canonical Allele Identifier: CA10614952

Gene: NDUFA10

Linked Data

• ClinVar Variation Id: 335175
• ClinVar RCV Id: RCV001539625
• dbSNP Id: rs138899326
• gnomAD v2: 2-240898611-A-AT
• gnomAD v3: 2-239959194-A-AT
• gnomAD v4: 2-239959194-A-AT
• MyVariant Identifiers: chr2:g.240898611_240898612insT (hg19) ; chr2:g.239959194_239959195insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.239959194_239959195insT , CM000664.2:g.239959194_239959195insT	GRCh38
NC_000002.11:g.240898611_240898612insT , CM000664.1:g.240898611_240898612insT	GRCh37
NC_000002.10:g.240547284_240547285insT	NCBI36
NG_031855.1:g.71208_71209insA
NG_031855.2:g.71208_71209insA

Transcript Alleles

HGVS	Amino-acid change
ENST00000252711.7:c.*1923_*1924insA MANE Select	ENSP00000252711.2:n.*1923_*1924insA
ENST00000476216.6:n.6130_6131insA
ENST00000676491.1:c.1000-158_1000-157insA	ENSP00000504528.1:n.1000-158_1000-157insA...
ENST00000676782.1:c.1000-20485_1000-20484insA	ENSP00000504717.1:n.1000-20485_1000-20484...
ENST00000676929.1:c.*96-158_*96-157insA	ENSP00000503956.1:n.*96-158_*96-157insA
ENST00000677057.1:n.4028+46015_4028+46016insA
ENST00000677155.1:c.*2180_*2181insA	ENSP00000502921.1:n.*2180_*2181insA
ENST00000677294.1:c.*1923_*1924insA	ENSP00000503461.1:n.*1923_*1924insA
ENST00000677324.1:n.5488_5489insA
ENST00000677395.1:c.*4687_*4688insA	ENSP00000502890.1:n.*4687_*4688insA
ENST00000677407.1:c.1000-8177_1000-8176insA	ENSP00000503141.1:n.1000-8177_1000-8176in...
ENST00000677692.1:n.4261-158_4261-157insA
ENST00000677764.1:c.*2302_*2303insA	ENSP00000504547.1:n.*2302_*2303insA
ENST00000677979.1:c.*2470_*2471insA	ENSP00000503341.1:n.*2470_*2471insA
ENST00000678158.1:c.*164-158_*164-157insA	ENSP00000504765.1:n.*164-158_*164-157insA...
ENST00000678188.1:n.6212_6213insA
ENST00000678455.1:c.*1923_*1924insA	ENSP00000504395.1:n.*1923_*1924insA
ENST00000678468.1:c.*2529_*2530insA	ENSP00000503925.1:n.*2529_*2530insA
ENST00000678562.1:c.*5826_*5827insA	ENSP00000502954.1:n.*5826_*5827insA
ENST00000678832.1:c.*2647_*2648insA	ENSP00000502992.1:n.*2647_*2648insA
ENST00000678914.1:c.*1923_*1924insA	ENSP00000504515.1:n.*1923_*1924insA
ENST00000679183.1:c.999+30879_999+30880insA	ENSP00000503016.1:n.999+30879_999+30880in...
ENST00000252711.6:c.*1923_*1924insA	ENSP00000252711.2:n.*1923_*1924insA
ENST00000419408.5:c.294+30879_294+30880insA	ENSP00000408055.1:n.294+30879_294+30880in...
ENST00000471378.1:n.82-158_82-157insA
NM_004544.3:c.*1923_*1924insA	NP_004535.1:n.*1923_*1924insA
NM_001322020.1:c.*1928_*1929insA	NP_001308949.1:n.*1928_*1929insA
NR_136155.1:n.6134_6135insA
NR_136156.1:n.6025_6026insA
NR_136157.1:n.5965_5966insA
NR_136158.1:n.4033+46015_4033+46016insA
NM_004544.4:c.*1923_*1924insA MANE Select	NP_004535.1:n.*1923_*1924insA
NM_001322020.2:c.*1928_*1929insA	NP_001308949.1:n.*1928_*1929insA
NR_136155.2:n.6074_6075insA
NR_136156.2:n.5965_5966insA
NR_136157.2:n.5905_5906insA
NR_136158.2:n.3973+46015_3973+46016insA