Canonical Allele Identifier: CA2496487368

Gene: NDUFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.206144924G= , CM000664.2:g.206144924G=	GRCh38
NC_000002.11:g.207009648G= , CM000664.1:g.207009648G=	GRCh37
NC_000002.10:g.206717893G=	NCBI36
NG_009248.1:g.19540C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233190.11:c.840C= MANE Select	ENSP00000233190.5:p.Asp280=
ENST00000233190.10:c.840C=	ENSP00000233190.5:p.Asp280=
ENST00000423725.5:c.669C=	ENSP00000397760.1:p.Asp223=
ENST00000432169.5:c.507C=	ENSP00000409689.1:p.Asp169=
ENST00000440274.5:c.732C=	ENSP00000409766.1:p.Asp244=
ENST00000449699.5:c.840C=	ENSP00000399912.1:p.Asp280=
ENST00000455934.6:c.882C=	ENSP00000392709.2:p.Asp294=
ENST00000457011.5:c.492C=	ENSP00000400976.1:p.Asp164=
NM_001199981.1:c.732C=	NP_001186910.1:p.Asp244=
NM_001199982.1:c.507C=	NP_001186911.1:p.Asp169=
NM_001199983.1:c.669C=	NP_001186912.1:p.Asp223=
NM_001199984.1:c.882C=	NP_001186913.1:p.Asp294=
NM_005006.6:c.840C=	NP_004997.4:p.Asp280=
XM_017004188.2:c.81C=	XP_016859677.1:p.Asp27=
NM_001199981.2:c.732C=	NP_001186910.1:p.Asp244=
NM_001199982.2:c.507C=	NP_001186911.1:p.Asp169=
NM_001199983.2:c.669C=	NP_001186912.1:p.Asp223=
NM_005006.7:c.840C= MANE Select	NP_004997.4:p.Asp280=
NM_001199984.2:c.882C=	NP_001186913.1:p.Asp294=