Canonical Allele Identifier: CA430952551

Gene: NDUFS1

Linked Data

• MyVariant Identifiers: chr2:g.207009639T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.206144915T>C , CM000664.2:g.206144915T>C	GRCh38
NC_000002.11:g.207009639T>C , CM000664.1:g.207009639T>C	GRCh37
NC_000002.10:g.206717884T>C	NCBI36
NG_009248.1:g.19549A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233190.11:c.849A>G MANE Select	ENSP00000233190.5:p.Glu283=
ENST00000233190.10:c.849A>G	ENSP00000233190.5:p.Glu283=
ENST00000423725.5:c.678A>G	ENSP00000397760.1:p.Glu226=
ENST00000432169.5:c.516A>G	ENSP00000409689.1:p.Glu172=
ENST00000440274.5:c.741A>G	ENSP00000409766.1:p.Glu247=
ENST00000449699.5:c.849A>G	ENSP00000399912.1:p.Glu283=
ENST00000455934.6:c.891A>G	ENSP00000392709.2:p.Glu297=
ENST00000457011.5:c.501A>G	ENSP00000400976.1:p.Glu167=
NM_001199981.1:c.741A>G	NP_001186910.1:p.Glu247=
NM_001199982.1:c.516A>G	NP_001186911.1:p.Glu172=
NM_001199983.1:c.678A>G	NP_001186912.1:p.Glu226=
NM_001199984.1:c.891A>G	NP_001186913.1:p.Glu297=
NM_005006.6:c.849A>G	NP_004997.4:p.Glu283=
XM_017004188.2:c.90A>G	XP_016859677.1:p.Glu30=
NM_001199981.2:c.741A>G	NP_001186910.1:p.Glu247=
NM_001199982.2:c.516A>G	NP_001186911.1:p.Glu172=
NM_001199983.2:c.678A>G	NP_001186912.1:p.Glu226=
NM_005006.7:c.849A>G MANE Select	NP_004997.4:p.Glu283=
NM_001199984.2:c.891A>G	NP_001186913.1:p.Glu297=