Canonical Allele Identifier: CA2496487382

Gene: NDUFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.206144952A= , CM000664.2:g.206144952A=	GRCh38
NC_000002.11:g.207009676A= , CM000664.1:g.207009676A=	GRCh37
NC_000002.10:g.206717921A=	NCBI36
NG_009248.1:g.19512T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233190.11:c.812T= MANE Select	ENSP00000233190.5:p.Met271=
ENST00000233190.10:c.812T=	ENSP00000233190.5:p.Met271=
ENST00000423725.5:c.641T=	ENSP00000397760.1:p.Met214=
ENST00000432169.5:c.479T=	ENSP00000409689.1:p.Met160=
ENST00000440274.5:c.704T=	ENSP00000409766.1:p.Met235=
ENST00000449699.5:c.812T=	ENSP00000399912.1:p.Met271=
ENST00000455934.6:c.854T=	ENSP00000392709.2:p.Met285=
ENST00000457011.5:c.464T=	ENSP00000400976.1:p.Met155=
NM_001199981.1:c.704T=	NP_001186910.1:p.Met235=
NM_001199982.1:c.479T=	NP_001186911.1:p.Met160=
NM_001199983.1:c.641T=	NP_001186912.1:p.Met214=
NM_001199984.1:c.854T=	NP_001186913.1:p.Met285=
NM_005006.6:c.812T=	NP_004997.4:p.Met271=
XM_017004188.2:c.53T=	XP_016859677.1:p.Met18=
NM_001199981.2:c.704T=	NP_001186910.1:p.Met235=
NM_001199982.2:c.479T=	NP_001186911.1:p.Met160=
NM_001199983.2:c.641T=	NP_001186912.1:p.Met214=
NM_005006.7:c.812T= MANE Select	NP_004997.4:p.Met271=
NM_001199984.2:c.854T=	NP_001186913.1:p.Met285=