Canonical Allele Identifier: CA350057712

Gene: NDUFS1

Linked Data

• MyVariant Identifiers: chr2:g.207009734C>G (hg19) ; chr2:g.206145010C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.206145010C>G , CM000664.2:g.206145010C>G	GRCh38
NC_000002.11:g.207009734C>G , CM000664.1:g.207009734C>G	GRCh37
NC_000002.10:g.206717979C>G	NCBI36
NG_009248.1:g.19454G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233190.11:c.754G>C MANE Select	ENSP00000233190.5:p.Asp252His
ENST00000233190.10:c.754G>C	ENSP00000233190.5:p.Asp252His
ENST00000423725.5:c.583G>C	ENSP00000397760.1:p.Asp195His
ENST00000432169.5:c.421G>C	ENSP00000409689.1:p.Asp141His
ENST00000440274.5:c.646G>C	ENSP00000409766.1:p.Asp216His
ENST00000449699.5:c.754G>C	ENSP00000399912.1:p.Asp252His
ENST00000455934.6:c.796G>C	ENSP00000392709.2:p.Asp266His
ENST00000457011.5:c.406G>C	ENSP00000400976.1:p.Asp136His
NM_001199981.1:c.646G>C	NP_001186910.1:p.Asp216His
NM_001199982.1:c.421G>C	NP_001186911.1:p.Asp141His
NM_001199983.1:c.583G>C	NP_001186912.1:p.Asp195His
NM_001199984.1:c.796G>C	NP_001186913.1:p.Asp266His
NM_005006.6:c.754G>C	NP_004997.4:p.Asp252His
XM_017004188.2:c.-6G>C	XP_016859677.1:n.-6G>C
NM_001199981.2:c.646G>C	NP_001186910.1:p.Asp216His
NM_001199982.2:c.421G>C	NP_001186911.1:p.Asp141His
NM_001199983.2:c.583G>C	NP_001186912.1:p.Asp195His
NM_005006.7:c.754G>C MANE Select	NP_004997.4:p.Asp252His
NM_001199984.2:c.796G>C	NP_001186913.1:p.Asp266His