Canonical Allele Identifier: CA350057505

Gene: NDUFS1

Linked Data

• gnomAD v4: 2-206144980-C-T
• MyVariant Identifiers: chr2:g.207009704C>T (hg19) ; chr2:g.206144980C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.206144980C>T , CM000664.2:g.206144980C>T	GRCh38
NC_000002.11:g.207009704C>T , CM000664.1:g.207009704C>T	GRCh37
NC_000002.10:g.206717949C>T	NCBI36
NG_009248.1:g.19484G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233190.11:c.784G>A MANE Select	ENSP00000233190.5:p.Val262Met
ENST00000233190.10:c.784G>A	ENSP00000233190.5:p.Val262Met
ENST00000423725.5:c.613G>A	ENSP00000397760.1:p.Val205Met
ENST00000432169.5:c.451G>A	ENSP00000409689.1:p.Val151Met
ENST00000440274.5:c.676G>A	ENSP00000409766.1:p.Val226Met
ENST00000449699.5:c.784G>A	ENSP00000399912.1:p.Val262Met
ENST00000455934.6:c.826G>A	ENSP00000392709.2:p.Val276Met
ENST00000457011.5:c.436G>A	ENSP00000400976.1:p.Val146Met
NM_001199981.1:c.676G>A	NP_001186910.1:p.Val226Met
NM_001199982.1:c.451G>A	NP_001186911.1:p.Val151Met
NM_001199983.1:c.613G>A	NP_001186912.1:p.Val205Met
NM_001199984.1:c.826G>A	NP_001186913.1:p.Val276Met
NM_005006.6:c.784G>A	NP_004997.4:p.Val262Met
XM_017004188.2:c.25G>A	XP_016859677.1:p.Val9Met
NM_001199981.2:c.676G>A	NP_001186910.1:p.Val226Met
NM_001199982.2:c.451G>A	NP_001186911.1:p.Val151Met
NM_001199983.2:c.613G>A	NP_001186912.1:p.Val205Met
NM_005006.7:c.784G>A MANE Select	NP_004997.4:p.Val262Met
NM_001199984.2:c.826G>A	NP_001186913.1:p.Val276Met