Canonical Allele Identifier: CA350043720

Gene: NDUFS1

Linked Data

• dbSNP Id: rs1317076909
• gnomAD v4: 2-206127939-T-C
• MyVariant Identifiers: chr2:g.206992663T>C (hg19) ; chr2:g.206127939T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.206127939T>C , CM000664.2:g.206127939T>C	GRCh38
NC_000002.11:g.206992663T>C , CM000664.1:g.206992663T>C	GRCh37
NC_000002.10:g.206700908T>C	NCBI36
NG_009248.1:g.36525A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233190.11:c.1742A>G MANE Select	ENSP00000233190.5:p.Asp581Gly
ENST00000233190.10:c.1742A>G	ENSP00000233190.5:p.Asp581Gly
ENST00000423725.5:c.1571A>G	ENSP00000397760.1:p.Asp524Gly
ENST00000432169.5:c.1409A>G	ENSP00000409689.1:p.Asp470Gly
ENST00000440274.5:c.1634A>G	ENSP00000409766.1:p.Asp545Gly
ENST00000449699.5:c.1742A>G	ENSP00000399912.1:p.Asp581Gly
ENST00000455934.6:c.1784A>G	ENSP00000392709.2:p.Asp595Gly
ENST00000457011.5:c.1394A>G	ENSP00000400976.1:p.Asp465Gly
ENST00000498520.1:n.214A>G
NM_001199981.1:c.1634A>G	NP_001186910.1:p.Asp545Gly
NM_001199982.1:c.1409A>G	NP_001186911.1:p.Asp470Gly
NM_001199983.1:c.1571A>G	NP_001186912.1:p.Asp524Gly
NM_001199984.1:c.1784A>G	NP_001186913.1:p.Asp595Gly
NM_005006.6:c.1742A>G	NP_004997.4:p.Asp581Gly
XM_017004188.2:c.983A>G	XP_016859677.1:p.Asp328Gly
NM_001199981.2:c.1634A>G	NP_001186910.1:p.Asp545Gly
NM_001199982.2:c.1409A>G	NP_001186911.1:p.Asp470Gly
NM_001199983.2:c.1571A>G	NP_001186912.1:p.Asp524Gly
NM_005006.7:c.1742A>G MANE Select	NP_004997.4:p.Asp581Gly
NM_001199984.2:c.1784A>G	NP_001186913.1:p.Asp595Gly