Canonical Allele Identifier: CA350056945

Gene: NDUFS1

Linked Data

• gnomAD v4: 2-206144908-T-C
• MyVariant Identifiers: chr2:g.207009632T>C (hg19) ; chr2:g.206144908T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.206144908T>C , CM000664.2:g.206144908T>C	GRCh38
NC_000002.11:g.207009632T>C , CM000664.1:g.207009632T>C	GRCh37
NC_000002.10:g.206717877T>C	NCBI36
NG_009248.1:g.19556A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233190.11:c.856A>G MANE Select	ENSP00000233190.5:p.Ile286Val
ENST00000233190.10:c.856A>G	ENSP00000233190.5:p.Ile286Val
ENST00000423725.5:c.685A>G	ENSP00000397760.1:p.Ile229Val
ENST00000432169.5:c.523A>G	ENSP00000409689.1:p.Ile175Val
ENST00000440274.5:c.748A>G	ENSP00000409766.1:p.Ile250Val
ENST00000449699.5:c.856A>G	ENSP00000399912.1:p.Ile286Val
ENST00000455934.6:c.898A>G	ENSP00000392709.2:p.Ile300Val
ENST00000457011.5:c.508A>G	ENSP00000400976.1:p.Ile170Val
NM_001199981.1:c.748A>G	NP_001186910.1:p.Ile250Val
NM_001199982.1:c.523A>G	NP_001186911.1:p.Ile175Val
NM_001199983.1:c.685A>G	NP_001186912.1:p.Ile229Val
NM_001199984.1:c.898A>G	NP_001186913.1:p.Ile300Val
NM_005006.6:c.856A>G	NP_004997.4:p.Ile286Val
XM_017004188.2:c.97A>G	XP_016859677.1:p.Ile33Val
NM_001199981.2:c.748A>G	NP_001186910.1:p.Ile250Val
NM_001199982.2:c.523A>G	NP_001186911.1:p.Ile175Val
NM_001199983.2:c.685A>G	NP_001186912.1:p.Ile229Val
NM_005006.7:c.856A>G MANE Select	NP_004997.4:p.Ile286Val
NM_001199984.2:c.898A>G	NP_001186913.1:p.Ile300Val