Canonical Allele Identifier: CA68047691
Community Standard Title: NM_004544.4(NDUFA10):c.*2133A>G
Gene: NDUFA10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.239958985T>C , CM000664.2:g.239958985T>C GRCh38
NC_000002.11:g.240898402T>C , CM000664.1:g.240898402T>C GRCh37
NC_000002.10:g.240547075T>C NCBI36
NG_031855.1:g.71418A>G
NG_031855.2:g.71418A>G

Transcript Alleles

HGVS Amino-acid Change
NM_004544.4:c.*2133A>G MANE Select NP_004535.1:n.*2133A>G
ENST00000252711.7:c.*2133A>G MANE Select ENSP00000252711.2:n.*2133A>G
NM_001322020.1:c.*2138A>G NP_001308949.1:n.*2138A>G
NM_001322020.2:c.*2138A>G NP_001308949.1:n.*2138A>G
NM_004544.3:c.*2133A>G NP_004535.1:n.*2133A>G
NR_136155.1:n.6344A>G
NR_136155.2:n.6284A>G
NR_136156.1:n.6235A>G
NR_136156.2:n.6175A>G
NR_136157.1:n.6175A>G
NR_136157.2:n.6115A>G
NR_136158.1:n.4034-45995A>G
NR_136158.2:n.3974-45995A>G
ENST00000252711.6:c.*2133A>G ENSP00000252711.2:n.*2133A>G
ENST00000419408.5:c.294+31089A>G ENSP00000408055.1:n.294+31089A>G
ENST00000471378.1:n.134A>G
ENST00000476216.6:n.6340A>G
ENST00000676491.1:c.1052A>G ENSP00000504528.1:p.Tyr351Cys
ENST00000676782.1:c.1000-20275A>G ENSP00000504717.1:n.1000-20275A>G
ENST00000676929.1:c.*148A>G ENSP00000503956.1:n.*148A>G
ENST00000677057.1:n.4029-45995A>G
ENST00000677155.1:c.*2390A>G ENSP00000502921.1:n.*2390A>G
ENST00000677294.1:c.*2133A>G ENSP00000503461.1:n.*2133A>G
ENST00000677324.1:n.5698A>G
ENST00000677395.1:c.*4897A>G ENSP00000502890.1:n.*4897A>G
ENST00000677407.1:c.1000-7967A>G ENSP00000503141.1:n.1000-7967A>G
ENST00000677692.1:n.4313A>G
ENST00000677764.1:c.*2512A>G ENSP00000504547.1:n.*2512A>G
ENST00000677979.1:c.*2680A>G ENSP00000503341.1:n.*2680A>G
ENST00000678158.1:c.*216A>G ENSP00000504765.1:n.*216A>G
ENST00000678188.1:n.6422A>G
ENST00000678455.1:c.*2133A>G ENSP00000504395.1:n.*2133A>G
ENST00000678468.1:c.*2739A>G ENSP00000503925.1:n.*2739A>G
ENST00000678562.1:c.*6036A>G ENSP00000502954.1:n.*6036A>G
ENST00000678832.1:c.*2857A>G ENSP00000502992.1:n.*2857A>G
ENST00000678914.1:c.*2133A>G ENSP00000504515.1:n.*2133A>G
ENST00000679183.1:c.999+31089A>G ENSP00000503016.1:n.999+31089A>G