Canonical Allele Identifier: CA430952383

Gene: NDUFS1

Linked Data

• MyVariant Identifiers: chr2:g.207009624A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.206144900A>G , CM000664.2:g.206144900A>G	GRCh38
NC_000002.11:g.207009624A>G , CM000664.1:g.207009624A>G	GRCh37
NC_000002.10:g.206717869A>G	NCBI36
NG_009248.1:g.19564T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233190.11:c.864T>C MANE Select	ENSP00000233190.5:p.Asp288=
ENST00000233190.10:c.864T>C	ENSP00000233190.5:p.Asp288=
ENST00000423725.5:c.693T>C	ENSP00000397760.1:p.Asp231=
ENST00000432169.5:c.531T>C	ENSP00000409689.1:p.Asp177=
ENST00000440274.5:c.756T>C	ENSP00000409766.1:p.Asp252=
ENST00000449699.5:c.864T>C	ENSP00000399912.1:p.Asp288=
ENST00000455934.6:c.906T>C	ENSP00000392709.2:p.Asp302=
ENST00000457011.5:c.516T>C	ENSP00000400976.1:p.Asp172=
NM_001199981.1:c.756T>C	NP_001186910.1:p.Asp252=
NM_001199982.1:c.531T>C	NP_001186911.1:p.Asp177=
NM_001199983.1:c.693T>C	NP_001186912.1:p.Asp231=
NM_001199984.1:c.906T>C	NP_001186913.1:p.Asp302=
NM_005006.6:c.864T>C	NP_004997.4:p.Asp288=
XM_017004188.2:c.105T>C	XP_016859677.1:p.Asp35=
NM_001199981.2:c.756T>C	NP_001186910.1:p.Asp252=
NM_001199982.2:c.531T>C	NP_001186911.1:p.Asp177=
NM_001199983.2:c.693T>C	NP_001186912.1:p.Asp231=
NM_005006.7:c.864T>C MANE Select	NP_004997.4:p.Asp288=
NM_001199984.2:c.906T>C	NP_001186913.1:p.Asp302=