Canonical Allele Identifier: CA2496487393

Gene: NDUFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.206144977C= , CM000664.2:g.206144977C=	GRCh38
NC_000002.11:g.207009701C= , CM000664.1:g.207009701C=	GRCh37
NC_000002.10:g.206717946C=	NCBI36
NG_009248.1:g.19487G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233190.11:c.787G= MANE Select	ENSP00000233190.5:p.Val263=
ENST00000233190.10:c.787G=	ENSP00000233190.5:p.Val263=
ENST00000423725.5:c.616G=	ENSP00000397760.1:p.Val206=
ENST00000432169.5:c.454G=	ENSP00000409689.1:p.Val152=
ENST00000440274.5:c.679G=	ENSP00000409766.1:p.Val227=
ENST00000449699.5:c.787G=	ENSP00000399912.1:p.Val263=
ENST00000455934.6:c.829G=	ENSP00000392709.2:p.Val277=
ENST00000457011.5:c.439G=	ENSP00000400976.1:p.Val147=
NM_001199981.1:c.679G=	NP_001186910.1:p.Val227=
NM_001199982.1:c.454G=	NP_001186911.1:p.Val152=
NM_001199983.1:c.616G=	NP_001186912.1:p.Val206=
NM_001199984.1:c.829G=	NP_001186913.1:p.Val277=
NM_005006.6:c.787G=	NP_004997.4:p.Val263=
XM_017004188.2:c.28G=	XP_016859677.1:p.Val10=
NM_001199981.2:c.679G=	NP_001186910.1:p.Val227=
NM_001199982.2:c.454G=	NP_001186911.1:p.Val152=
NM_001199983.2:c.616G=	NP_001186912.1:p.Val206=
NM_005006.7:c.787G= MANE Select	NP_004997.4:p.Val263=
NM_001199984.2:c.829G=	NP_001186913.1:p.Val277=