Canonical Allele Identifier: CA350043597

Gene: NDUFS1

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233190.11:c.1760C>T MANE Select	ENSP00000233190.5:p.Ala587Val
ENST00000233190.10:c.1760C>T	ENSP00000233190.5:p.Ala587Val
ENST00000423725.5:c.1589C>T	ENSP00000397760.1:p.Ala530Val
ENST00000432169.5:c.1427C>T	ENSP00000409689.1:p.Ala476Val
ENST00000440274.5:c.1652C>T	ENSP00000409766.1:p.Ala551Val
ENST00000449699.5:c.1760C>T	ENSP00000399912.1:p.Ala587Val
ENST00000455934.6:c.1802C>T	ENSP00000392709.2:p.Ala601Val
ENST00000457011.5:c.1412C>T	ENSP00000400976.1:p.Ala471Val
ENST00000498520.1:n.232C>T
NM_001199981.1:c.1652C>T	NP_001186910.1:p.Ala551Val
NM_001199982.1:c.1427C>T	NP_001186911.1:p.Ala476Val
NM_001199983.1:c.1589C>T	NP_001186912.1:p.Ala530Val
NM_001199984.1:c.1802C>T	NP_001186913.1:p.Ala601Val
NM_005006.6:c.1760C>T	NP_004997.4:p.Ala587Val
XM_017004188.2:c.1001C>T	XP_016859677.1:p.Ala334Val
NM_001199981.2:c.1652C>T	NP_001186910.1:p.Ala551Val
NM_001199982.2:c.1427C>T	NP_001186911.1:p.Ala476Val
NM_001199983.2:c.1589C>T	NP_001186912.1:p.Ala530Val
NM_005006.7:c.1760C>T MANE Select	NP_004997.4:p.Ala587Val
NM_001199984.2:c.1802C>T	NP_001186913.1:p.Ala601Val