Canonical Allele Identifier: CA2496486031

Gene: NDUFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.206141952T= , CM000664.2:g.206141952T=	GRCh38
NC_000002.11:g.207006676T= , CM000664.1:g.207006676T=	GRCh37
NC_000002.10:g.206714921T=	NCBI36
NG_009248.1:g.22512A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233190.11:c.1251A= MANE Select	ENSP00000233190.5:p.Arg417=
ENST00000233190.10:c.1251A=	ENSP00000233190.5:p.Arg417=
ENST00000423725.5:c.1080A=	ENSP00000397760.1:p.Arg360=
ENST00000432169.5:c.918A=	ENSP00000409689.1:p.Arg306=
ENST00000440274.5:c.1143A=	ENSP00000409766.1:p.Arg381=
ENST00000449699.5:c.1251A=	ENSP00000399912.1:p.Arg417=
ENST00000455934.6:c.1293A=	ENSP00000392709.2:p.Arg431=
ENST00000457011.5:c.903A=	ENSP00000400976.1:p.Arg301=
NM_001199981.1:c.1143A=	NP_001186910.1:p.Arg381=
NM_001199982.1:c.918A=	NP_001186911.1:p.Arg306=
NM_001199983.1:c.1080A=	NP_001186912.1:p.Arg360=
NM_001199984.1:c.1293A=	NP_001186913.1:p.Arg431=
NM_005006.6:c.1251A=	NP_004997.4:p.Arg417=
XM_017004188.2:c.492A=	XP_016859677.1:p.Arg164=
NM_001199981.2:c.1143A=	NP_001186910.1:p.Arg381=
NM_001199982.2:c.918A=	NP_001186911.1:p.Arg306=
NM_001199983.2:c.1080A=	NP_001186912.1:p.Arg360=
NM_005006.7:c.1251A= MANE Select	NP_004997.4:p.Arg417=
NM_001199984.2:c.1293A=	NP_001186913.1:p.Arg431=