Canonical Allele Identifier: CA2496487380

Gene: NDUFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.206144949C= , CM000664.2:g.206144949C=	GRCh38
NC_000002.11:g.207009673C= , CM000664.1:g.207009673C=	GRCh37
NC_000002.10:g.206717918C=	NCBI36
NG_009248.1:g.19515G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233190.11:c.815G= MANE Select	ENSP00000233190.5:p.Arg272=
ENST00000233190.10:c.815G=	ENSP00000233190.5:p.Arg272=
ENST00000423725.5:c.644G=	ENSP00000397760.1:p.Arg215=
ENST00000432169.5:c.482G=	ENSP00000409689.1:p.Arg161=
ENST00000440274.5:c.707G=	ENSP00000409766.1:p.Arg236=
ENST00000449699.5:c.815G=	ENSP00000399912.1:p.Arg272=
ENST00000455934.6:c.857G=	ENSP00000392709.2:p.Arg286=
ENST00000457011.5:c.467G=	ENSP00000400976.1:p.Arg156=
NM_001199981.1:c.707G=	NP_001186910.1:p.Arg236=
NM_001199982.1:c.482G=	NP_001186911.1:p.Arg161=
NM_001199983.1:c.644G=	NP_001186912.1:p.Arg215=
NM_001199984.1:c.857G=	NP_001186913.1:p.Arg286=
NM_005006.6:c.815G=	NP_004997.4:p.Arg272=
XM_017004188.2:c.56G=	XP_016859677.1:p.Arg19=
NM_001199981.2:c.707G=	NP_001186910.1:p.Arg236=
NM_001199982.2:c.482G=	NP_001186911.1:p.Arg161=
NM_001199983.2:c.644G=	NP_001186912.1:p.Arg215=
NM_005006.7:c.815G= MANE Select	NP_004997.4:p.Arg272=
NM_001199984.2:c.857G=	NP_001186913.1:p.Arg286=