Canonical Allele Identifier: CA2496487379

Gene: NDUFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.206144947T= , CM000664.2:g.206144947T=	GRCh38
NC_000002.11:g.207009671T= , CM000664.1:g.207009671T=	GRCh37
NC_000002.10:g.206717916T=	NCBI36
NG_009248.1:g.19517A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233190.11:c.817A= MANE Select	ENSP00000233190.5:p.Ile273=
ENST00000233190.10:c.817A=	ENSP00000233190.5:p.Ile273=
ENST00000423725.5:c.646A=	ENSP00000397760.1:p.Ile216=
ENST00000432169.5:c.484A=	ENSP00000409689.1:p.Ile162=
ENST00000440274.5:c.709A=	ENSP00000409766.1:p.Ile237=
ENST00000449699.5:c.817A=	ENSP00000399912.1:p.Ile273=
ENST00000455934.6:c.859A=	ENSP00000392709.2:p.Ile287=
ENST00000457011.5:c.469A=	ENSP00000400976.1:p.Ile157=
NM_001199981.1:c.709A=	NP_001186910.1:p.Ile237=
NM_001199982.1:c.484A=	NP_001186911.1:p.Ile162=
NM_001199983.1:c.646A=	NP_001186912.1:p.Ile216=
NM_001199984.1:c.859A=	NP_001186913.1:p.Ile287=
NM_005006.6:c.817A=	NP_004997.4:p.Ile273=
XM_017004188.2:c.58A=	XP_016859677.1:p.Ile20=
NM_001199981.2:c.709A=	NP_001186910.1:p.Ile237=
NM_001199982.2:c.484A=	NP_001186911.1:p.Ile162=
NM_001199983.2:c.646A=	NP_001186912.1:p.Ile216=
NM_005006.7:c.817A= MANE Select	NP_004997.4:p.Ile273=
NM_001199984.2:c.859A=	NP_001186913.1:p.Ile287=