Canonical Allele Identifier: CA430953482

Gene: NDUFS1

Linked Data

• dbSNP Id: rs1260183814
• gnomAD v2: 2-207009729-T-C
• gnomAD v4: 2-206145005-T-C
• MyVariant Identifiers: chr2:g.207009729T>C (hg19) ; chr2:g.206145005T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.206145005T>C , CM000664.2:g.206145005T>C	GRCh38
NC_000002.11:g.207009729T>C , CM000664.1:g.207009729T>C	GRCh37
NC_000002.10:g.206717974T>C	NCBI36
NG_009248.1:g.19459A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233190.11:c.759A>G MANE Select	ENSP00000233190.5:p.Val253=
ENST00000233190.10:c.759A>G	ENSP00000233190.5:p.Val253=
ENST00000423725.5:c.588A>G	ENSP00000397760.1:p.Val196=
ENST00000432169.5:c.426A>G	ENSP00000409689.1:p.Val142=
ENST00000440274.5:c.651A>G	ENSP00000409766.1:p.Val217=
ENST00000449699.5:c.759A>G	ENSP00000399912.1:p.Val253=
ENST00000455934.6:c.801A>G	ENSP00000392709.2:p.Val267=
ENST00000457011.5:c.411A>G	ENSP00000400976.1:p.Val137=
NM_001199981.1:c.651A>G	NP_001186910.1:p.Val217=
NM_001199982.1:c.426A>G	NP_001186911.1:p.Val142=
NM_001199983.1:c.588A>G	NP_001186912.1:p.Val196=
NM_001199984.1:c.801A>G	NP_001186913.1:p.Val267=
NM_005006.6:c.759A>G	NP_004997.4:p.Val253=
XM_017004188.2:c.-1A>G	XP_016859677.1:n.-1A>G
NM_001199981.2:c.651A>G	NP_001186910.1:p.Val217=
NM_001199982.2:c.426A>G	NP_001186911.1:p.Val142=
NM_001199983.2:c.588A>G	NP_001186912.1:p.Val196=
NM_005006.7:c.759A>G MANE Select	NP_004997.4:p.Val253=
NM_001199984.2:c.801A>G	NP_001186913.1:p.Val267=