Canonical Allele Identifier: CA350043601

Gene: NDUFS1

Linked Data

• MyVariant Identifiers: chr2:g.206992645G>T (hg19) ; chr2:g.206127921G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.206127921G>T , CM000664.2:g.206127921G>T	GRCh38
NC_000002.11:g.206992645G>T , CM000664.1:g.206992645G>T	GRCh37
NC_000002.10:g.206700890G>T	NCBI36
NG_009248.1:g.36543C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233190.11:c.1760C>A MANE Select	ENSP00000233190.5:p.Ala587Asp
ENST00000233190.10:c.1760C>A	ENSP00000233190.5:p.Ala587Asp
ENST00000423725.5:c.1589C>A	ENSP00000397760.1:p.Ala530Asp
ENST00000432169.5:c.1427C>A	ENSP00000409689.1:p.Ala476Asp
ENST00000440274.5:c.1652C>A	ENSP00000409766.1:p.Ala551Asp
ENST00000449699.5:c.1760C>A	ENSP00000399912.1:p.Ala587Asp
ENST00000455934.6:c.1802C>A	ENSP00000392709.2:p.Ala601Asp
ENST00000457011.5:c.1412C>A	ENSP00000400976.1:p.Ala471Asp
ENST00000498520.1:n.232C>A
NM_001199981.1:c.1652C>A	NP_001186910.1:p.Ala551Asp
NM_001199982.1:c.1427C>A	NP_001186911.1:p.Ala476Asp
NM_001199983.1:c.1589C>A	NP_001186912.1:p.Ala530Asp
NM_001199984.1:c.1802C>A	NP_001186913.1:p.Ala601Asp
NM_005006.6:c.1760C>A	NP_004997.4:p.Ala587Asp
XM_017004188.2:c.1001C>A	XP_016859677.1:p.Ala334Asp
NM_001199981.2:c.1652C>A	NP_001186910.1:p.Ala551Asp
NM_001199982.2:c.1427C>A	NP_001186911.1:p.Ala476Asp
NM_001199983.2:c.1589C>A	NP_001186912.1:p.Ala530Asp
NM_005006.7:c.1760C>A MANE Select	NP_004997.4:p.Ala587Asp
NM_001199984.2:c.1802C>A	NP_001186913.1:p.Ala601Asp