Canonical Allele Identifier: CA2070426

Gene: NDUFS1

Linked Data

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.206132982C>T , CM000664.2:g.206132982C>T	GRCh38
NC_000002.11:g.206997706C>T , CM000664.1:g.206997706C>T	GRCh37
NC_000002.10:g.206705951C>T	NCBI36
NG_009248.1:g.31482G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233190.11:c.1516G>A MANE Select	ENSP00000233190.5:p.Val506Ile
ENST00000233190.10:c.1516G>A	ENSP00000233190.5:p.Val506Ile
ENST00000423725.5:c.1345G>A	ENSP00000397760.1:p.Val449Ile
ENST00000432169.5:c.1183G>A	ENSP00000409689.1:p.Val395Ile
ENST00000440274.5:c.1408G>A	ENSP00000409766.1:p.Val470Ile
ENST00000449699.5:c.1516G>A	ENSP00000399912.1:p.Val506Ile
ENST00000455934.6:c.1558G>A	ENSP00000392709.2:p.Val520Ile
ENST00000457011.5:c.1168G>A	ENSP00000400976.1:p.Val390Ile
NM_001199981.1:c.1408G>A	NP_001186910.1:p.Val470Ile
NM_001199982.1:c.1183G>A	NP_001186911.1:p.Val395Ile
NM_001199983.1:c.1345G>A	NP_001186912.1:p.Val449Ile
NM_001199984.1:c.1558G>A	NP_001186913.1:p.Val520Ile
NM_005006.6:c.1516G>A	NP_004997.4:p.Val506Ile
XM_017004188.2:c.757G>A	XP_016859677.1:p.Val253Ile
NM_001199981.2:c.1408G>A	NP_001186910.1:p.Val470Ile
NM_001199982.2:c.1183G>A	NP_001186911.1:p.Val395Ile
NM_001199983.2:c.1345G>A	NP_001186912.1:p.Val449Ile
NM_005006.7:c.1516G>A MANE Select	NP_004997.4:p.Val506Ile
NM_001199984.2:c.1558G>A	NP_001186913.1:p.Val520Ile