Canonical Allele Identifier: CA350056955

Gene: NDUFS1

Linked Data

• MyVariant Identifiers: chr2:g.207009633C>G (hg19) ; chr2:g.206144909C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.206144909C>G , CM000664.2:g.206144909C>G	GRCh38
NC_000002.11:g.207009633C>G , CM000664.1:g.207009633C>G	GRCh37
NC_000002.10:g.206717878C>G	NCBI36
NG_009248.1:g.19555G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233190.11:c.855G>C MANE Select	ENSP00000233190.5:p.Trp285Cys
ENST00000233190.10:c.855G>C	ENSP00000233190.5:p.Trp285Cys
ENST00000423725.5:c.684G>C	ENSP00000397760.1:p.Trp228Cys
ENST00000432169.5:c.522G>C	ENSP00000409689.1:p.Trp174Cys
ENST00000440274.5:c.747G>C	ENSP00000409766.1:p.Trp249Cys
ENST00000449699.5:c.855G>C	ENSP00000399912.1:p.Trp285Cys
ENST00000455934.6:c.897G>C	ENSP00000392709.2:p.Trp299Cys
ENST00000457011.5:c.507G>C	ENSP00000400976.1:p.Trp169Cys
NM_001199981.1:c.747G>C	NP_001186910.1:p.Trp249Cys
NM_001199982.1:c.522G>C	NP_001186911.1:p.Trp174Cys
NM_001199983.1:c.684G>C	NP_001186912.1:p.Trp228Cys
NM_001199984.1:c.897G>C	NP_001186913.1:p.Trp299Cys
NM_005006.6:c.855G>C	NP_004997.4:p.Trp285Cys
XM_017004188.2:c.96G>C	XP_016859677.1:p.Trp32Cys
NM_001199981.2:c.747G>C	NP_001186910.1:p.Trp249Cys
NM_001199982.2:c.522G>C	NP_001186911.1:p.Trp174Cys
NM_001199983.2:c.684G>C	NP_001186912.1:p.Trp228Cys
NM_005006.7:c.855G>C MANE Select	NP_004997.4:p.Trp285Cys
NM_001199984.2:c.897G>C	NP_001186913.1:p.Trp299Cys