Canonical Allele Identifier: CA350043669

Gene: NDUFS1

Linked Data

• MyVariant Identifiers: chr2:g.206992656A>C (hg19) ; chr2:g.206127932A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.206127932A>C , CM000664.2:g.206127932A>C	GRCh38
NC_000002.11:g.206992656A>C , CM000664.1:g.206992656A>C	GRCh37
NC_000002.10:g.206700901A>C	NCBI36
NG_009248.1:g.36532T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233190.11:c.1749T>G MANE Select	ENSP00000233190.5:p.Ile583Met
ENST00000233190.10:c.1749T>G	ENSP00000233190.5:p.Ile583Met
ENST00000423725.5:c.1578T>G	ENSP00000397760.1:p.Ile526Met
ENST00000432169.5:c.1416T>G	ENSP00000409689.1:p.Ile472Met
ENST00000440274.5:c.1641T>G	ENSP00000409766.1:p.Ile547Met
ENST00000449699.5:c.1749T>G	ENSP00000399912.1:p.Ile583Met
ENST00000455934.6:c.1791T>G	ENSP00000392709.2:p.Ile597Met
ENST00000457011.5:c.1401T>G	ENSP00000400976.1:p.Ile467Met
ENST00000498520.1:n.221T>G
NM_001199981.1:c.1641T>G	NP_001186910.1:p.Ile547Met
NM_001199982.1:c.1416T>G	NP_001186911.1:p.Ile472Met
NM_001199983.1:c.1578T>G	NP_001186912.1:p.Ile526Met
NM_001199984.1:c.1791T>G	NP_001186913.1:p.Ile597Met
NM_005006.6:c.1749T>G	NP_004997.4:p.Ile583Met
XM_017004188.2:c.990T>G	XP_016859677.1:p.Ile330Met
NM_001199981.2:c.1641T>G	NP_001186910.1:p.Ile547Met
NM_001199982.2:c.1416T>G	NP_001186911.1:p.Ile472Met
NM_001199983.2:c.1578T>G	NP_001186912.1:p.Ile526Met
NM_005006.7:c.1749T>G MANE Select	NP_004997.4:p.Ile583Met
NM_001199984.2:c.1791T>G	NP_001186913.1:p.Ile597Met