Canonical Allele Identifier: CA430943177

Gene: NDUFS1

Linked Data

• MyVariant Identifiers: chr2:g.206992602A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.206127878A>T , CM000664.2:g.206127878A>T	GRCh38
NC_000002.11:g.206992602A>T , CM000664.1:g.206992602A>T	GRCh37
NC_000002.10:g.206700847A>T	NCBI36
NG_009248.1:g.36586T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233190.11:c.1803T>A MANE Select	ENSP00000233190.5:p.Gly601=
ENST00000233190.10:c.1803T>A	ENSP00000233190.5:p.Gly601=
ENST00000423725.5:c.1632T>A	ENSP00000397760.1:p.Gly544=
ENST00000432169.5:c.1470T>A	ENSP00000409689.1:p.Gly490=
ENST00000440274.5:c.1695T>A	ENSP00000409766.1:p.Gly565=
ENST00000449699.5:c.1803T>A	ENSP00000399912.1:p.Gly601=
ENST00000455934.6:c.1845T>A	ENSP00000392709.2:p.Gly615=
ENST00000457011.5:c.1455T>A	ENSP00000400976.1:p.Gly485=
ENST00000498520.1:n.275T>A
NM_001199981.1:c.1695T>A	NP_001186910.1:p.Gly565=
NM_001199982.1:c.1470T>A	NP_001186911.1:p.Gly490=
NM_001199983.1:c.1632T>A	NP_001186912.1:p.Gly544=
NM_001199984.1:c.1845T>A	NP_001186913.1:p.Gly615=
NM_005006.6:c.1803T>A	NP_004997.4:p.Gly601=
XM_017004188.2:c.1044T>A	XP_016859677.1:p.Gly348=
NM_001199981.2:c.1695T>A	NP_001186910.1:p.Gly565=
NM_001199982.2:c.1470T>A	NP_001186911.1:p.Gly490=
NM_001199983.2:c.1632T>A	NP_001186912.1:p.Gly544=
NM_005006.7:c.1803T>A MANE Select	NP_004997.4:p.Gly601=
NM_001199984.2:c.1845T>A	NP_001186913.1:p.Gly615=