Canonical Allele Identifier: CA350056903

Gene: NDUFS1

Linked Data

• dbSNP Id: rs1363601217
• MyVariant Identifiers: chr2:g.207009626C>G (hg19) ; chr2:g.206144902C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.206144902C>G , CM000664.2:g.206144902C>G	GRCh38
NC_000002.11:g.207009626C>G , CM000664.1:g.207009626C>G	GRCh37
NC_000002.10:g.206717871C>G	NCBI36
NG_009248.1:g.19562G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233190.11:c.862G>C MANE Select	ENSP00000233190.5:p.Asp288His
ENST00000233190.10:c.862G>C	ENSP00000233190.5:p.Asp288His
ENST00000423725.5:c.691G>C	ENSP00000397760.1:p.Asp231His
ENST00000432169.5:c.529G>C	ENSP00000409689.1:p.Asp177His
ENST00000440274.5:c.754G>C	ENSP00000409766.1:p.Asp252His
ENST00000449699.5:c.862G>C	ENSP00000399912.1:p.Asp288His
ENST00000455934.6:c.904G>C	ENSP00000392709.2:p.Asp302His
ENST00000457011.5:c.514G>C	ENSP00000400976.1:p.Asp172His
NM_001199981.1:c.754G>C	NP_001186910.1:p.Asp252His
NM_001199982.1:c.529G>C	NP_001186911.1:p.Asp177His
NM_001199983.1:c.691G>C	NP_001186912.1:p.Asp231His
NM_001199984.1:c.904G>C	NP_001186913.1:p.Asp302His
NM_005006.6:c.862G>C	NP_004997.4:p.Asp288His
XM_017004188.2:c.103G>C	XP_016859677.1:p.Asp35His
NM_001199981.2:c.754G>C	NP_001186910.1:p.Asp252His
NM_001199982.2:c.529G>C	NP_001186911.1:p.Asp177His
NM_001199983.2:c.691G>C	NP_001186912.1:p.Asp231His
NM_005006.7:c.862G>C MANE Select	NP_004997.4:p.Asp288His
NM_001199984.2:c.904G>C	NP_001186913.1:p.Asp302His