Canonical Allele Identifier: CA350057500

Gene: NDUFS1

Linked Data

• MyVariant Identifiers: chr2:g.207009704C>A (hg19) ; chr2:g.206144980C>A (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233190.11:c.784G>T MANE Select	ENSP00000233190.5:p.Val262Leu
ENST00000233190.10:c.784G>T	ENSP00000233190.5:p.Val262Leu
ENST00000423725.5:c.613G>T	ENSP00000397760.1:p.Val205Leu
ENST00000432169.5:c.451G>T	ENSP00000409689.1:p.Val151Leu
ENST00000440274.5:c.676G>T	ENSP00000409766.1:p.Val226Leu
ENST00000449699.5:c.784G>T	ENSP00000399912.1:p.Val262Leu
ENST00000455934.6:c.826G>T	ENSP00000392709.2:p.Val276Leu
ENST00000457011.5:c.436G>T	ENSP00000400976.1:p.Val146Leu
NM_001199981.1:c.676G>T	NP_001186910.1:p.Val226Leu
NM_001199982.1:c.451G>T	NP_001186911.1:p.Val151Leu
NM_001199983.1:c.613G>T	NP_001186912.1:p.Val205Leu
NM_001199984.1:c.826G>T	NP_001186913.1:p.Val276Leu
NM_005006.6:c.784G>T	NP_004997.4:p.Val262Leu
XM_017004188.2:c.25G>T	XP_016859677.1:p.Val9Leu
NM_001199981.2:c.676G>T	NP_001186910.1:p.Val226Leu
NM_001199982.2:c.451G>T	NP_001186911.1:p.Val151Leu
NM_001199983.2:c.613G>T	NP_001186912.1:p.Val205Leu
NM_005006.7:c.784G>T MANE Select	NP_004997.4:p.Val262Leu
NM_001199984.2:c.826G>T	NP_001186913.1:p.Val276Leu