Canonical Allele Identifier: CA430943475

Gene: NDUFS1

Linked Data

• ClinVar Variation Id: 1978898
• ClinVar RCV Id: RCV002775166
• gnomAD v4: 2-206127938-A-G
• MyVariant Identifiers: chr2:g.206992662A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.206127938A>G , CM000664.2:g.206127938A>G	GRCh38
NC_000002.11:g.206992662A>G , CM000664.1:g.206992662A>G	GRCh37
NC_000002.10:g.206700907A>G	NCBI36
NG_009248.1:g.36526T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233190.11:c.1743T>C MANE Select	ENSP00000233190.5:p.Asp581=
ENST00000233190.10:c.1743T>C	ENSP00000233190.5:p.Asp581=
ENST00000423725.5:c.1572T>C	ENSP00000397760.1:p.Asp524=
ENST00000432169.5:c.1410T>C	ENSP00000409689.1:p.Asp470=
ENST00000440274.5:c.1635T>C	ENSP00000409766.1:p.Asp545=
ENST00000449699.5:c.1743T>C	ENSP00000399912.1:p.Asp581=
ENST00000455934.6:c.1785T>C	ENSP00000392709.2:p.Asp595=
ENST00000457011.5:c.1395T>C	ENSP00000400976.1:p.Asp465=
ENST00000498520.1:n.215T>C
NM_001199981.1:c.1635T>C	NP_001186910.1:p.Asp545=
NM_001199982.1:c.1410T>C	NP_001186911.1:p.Asp470=
NM_001199983.1:c.1572T>C	NP_001186912.1:p.Asp524=
NM_001199984.1:c.1785T>C	NP_001186913.1:p.Asp595=
NM_005006.6:c.1743T>C	NP_004997.4:p.Asp581=
XM_017004188.2:c.984T>C	XP_016859677.1:p.Asp328=
NM_001199981.2:c.1635T>C	NP_001186910.1:p.Asp545=
NM_001199982.2:c.1410T>C	NP_001186911.1:p.Asp470=
NM_001199983.2:c.1572T>C	NP_001186912.1:p.Asp524=
NM_005006.7:c.1743T>C MANE Select	NP_004997.4:p.Asp581=
NM_001199984.2:c.1785T>C	NP_001186913.1:p.Asp595=