Canonical Allele Identifier: CA430952523

Gene: NDUFS1

Linked Data

• MyVariant Identifiers: chr2:g.207009636C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.206144912C>T , CM000664.2:g.206144912C>T	GRCh38
NC_000002.11:g.207009636C>T , CM000664.1:g.207009636C>T	GRCh37
NC_000002.10:g.206717881C>T	NCBI36
NG_009248.1:g.19552G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233190.11:c.852G>A MANE Select	ENSP00000233190.5:p.Glu284=
ENST00000233190.10:c.852G>A	ENSP00000233190.5:p.Glu284=
ENST00000423725.5:c.681G>A	ENSP00000397760.1:p.Glu227=
ENST00000432169.5:c.519G>A	ENSP00000409689.1:p.Glu173=
ENST00000440274.5:c.744G>A	ENSP00000409766.1:p.Glu248=
ENST00000449699.5:c.852G>A	ENSP00000399912.1:p.Glu284=
ENST00000455934.6:c.894G>A	ENSP00000392709.2:p.Glu298=
ENST00000457011.5:c.504G>A	ENSP00000400976.1:p.Glu168=
NM_001199981.1:c.744G>A	NP_001186910.1:p.Glu248=
NM_001199982.1:c.519G>A	NP_001186911.1:p.Glu173=
NM_001199983.1:c.681G>A	NP_001186912.1:p.Glu227=
NM_001199984.1:c.894G>A	NP_001186913.1:p.Glu298=
NM_005006.6:c.852G>A	NP_004997.4:p.Glu284=
XM_017004188.2:c.93G>A	XP_016859677.1:p.Glu31=
NM_001199981.2:c.744G>A	NP_001186910.1:p.Glu248=
NM_001199982.2:c.519G>A	NP_001186911.1:p.Glu173=
NM_001199983.2:c.681G>A	NP_001186912.1:p.Glu227=
NM_005006.7:c.852G>A MANE Select	NP_004997.4:p.Glu284=
NM_001199984.2:c.894G>A	NP_001186913.1:p.Glu298=