Canonical Allele Identifier: CA350057489

Gene: NDUFS1

Linked Data

• dbSNP Id: rs1692102744
• MyVariant Identifiers: chr2:g.207009701C>T (hg19) ; chr2:g.206144977C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.206144977C>T , CM000664.2:g.206144977C>T	GRCh38
NC_000002.11:g.207009701C>T , CM000664.1:g.207009701C>T	GRCh37
NC_000002.10:g.206717946C>T	NCBI36
NG_009248.1:g.19487G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233190.11:c.787G>A MANE Select	ENSP00000233190.5:p.Val263Ile
ENST00000233190.10:c.787G>A	ENSP00000233190.5:p.Val263Ile
ENST00000423725.5:c.616G>A	ENSP00000397760.1:p.Val206Ile
ENST00000432169.5:c.454G>A	ENSP00000409689.1:p.Val152Ile
ENST00000440274.5:c.679G>A	ENSP00000409766.1:p.Val227Ile
ENST00000449699.5:c.787G>A	ENSP00000399912.1:p.Val263Ile
ENST00000455934.6:c.829G>A	ENSP00000392709.2:p.Val277Ile
ENST00000457011.5:c.439G>A	ENSP00000400976.1:p.Val147Ile
NM_001199981.1:c.679G>A	NP_001186910.1:p.Val227Ile
NM_001199982.1:c.454G>A	NP_001186911.1:p.Val152Ile
NM_001199983.1:c.616G>A	NP_001186912.1:p.Val206Ile
NM_001199984.1:c.829G>A	NP_001186913.1:p.Val277Ile
NM_005006.6:c.787G>A	NP_004997.4:p.Val263Ile
XM_017004188.2:c.28G>A	XP_016859677.1:p.Val10Ile
NM_001199981.2:c.679G>A	NP_001186910.1:p.Val227Ile
NM_001199982.2:c.454G>A	NP_001186911.1:p.Val152Ile
NM_001199983.2:c.616G>A	NP_001186912.1:p.Val206Ile
NM_005006.7:c.787G>A MANE Select	NP_004997.4:p.Val263Ile
NM_001199984.2:c.829G>A	NP_001186913.1:p.Val277Ile