Canonical Allele Identifier: CA2496487369
Gene: NDUFS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.206144927C= , CM000664.2:g.206144927C= GRCh38
NC_000002.11:g.207009651C= , CM000664.1:g.207009651C= GRCh37
NC_000002.10:g.206717896C= NCBI36
NG_009248.1:g.19537G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000233190.11:c.837G= MANE Select ENSP00000233190.5:p.Glu279=
ENST00000233190.10:c.837G= ENSP00000233190.5:p.Glu279=
ENST00000423725.5:c.666G= ENSP00000397760.1:p.Glu222=
ENST00000432169.5:c.504G= ENSP00000409689.1:p.Glu168=
ENST00000440274.5:c.729G= ENSP00000409766.1:p.Glu243=
ENST00000449699.5:c.837G= ENSP00000399912.1:p.Glu279=
ENST00000455934.6:c.879G= ENSP00000392709.2:p.Glu293=
ENST00000457011.5:c.489G= ENSP00000400976.1:p.Glu163=
NM_001199981.1:c.729G= NP_001186910.1:p.Glu243=
NM_001199982.1:c.504G= NP_001186911.1:p.Glu168=
NM_001199983.1:c.666G= NP_001186912.1:p.Glu222=
NM_001199984.1:c.879G= NP_001186913.1:p.Glu293=
NM_005006.6:c.837G= NP_004997.4:p.Glu279=
XM_017004188.2:c.78G= XP_016859677.1:p.Glu26=
NM_001199981.2:c.729G= NP_001186910.1:p.Glu243=
NM_001199982.2:c.504G= NP_001186911.1:p.Glu168=
NM_001199983.2:c.666G= NP_001186912.1:p.Glu222=
NM_005006.7:c.837G= MANE Select NP_004997.4:p.Glu279=
NM_001199984.2:c.879G= NP_001186913.1:p.Glu293=