Canonical Allele Identifier: CA2496487367

Gene: NDUFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.206144923T= , CM000664.2:g.206144923T=	GRCh38
NC_000002.11:g.207009647T= , CM000664.1:g.207009647T=	GRCh37
NC_000002.10:g.206717892T=	NCBI36
NG_009248.1:g.19541A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000233190.11:c.841A= MANE Select	ENSP00000233190.5:p.Ile281=
ENST00000233190.10:c.841A=	ENSP00000233190.5:p.Ile281=
ENST00000423725.5:c.670A=	ENSP00000397760.1:p.Ile224=
ENST00000432169.5:c.508A=	ENSP00000409689.1:p.Ile170=
ENST00000440274.5:c.733A=	ENSP00000409766.1:p.Ile245=
ENST00000449699.5:c.841A=	ENSP00000399912.1:p.Ile281=
ENST00000455934.6:c.883A=	ENSP00000392709.2:p.Ile295=
ENST00000457011.5:c.493A=	ENSP00000400976.1:p.Ile165=
NM_001199981.1:c.733A=	NP_001186910.1:p.Ile245=
NM_001199982.1:c.508A=	NP_001186911.1:p.Ile170=
NM_001199983.1:c.670A=	NP_001186912.1:p.Ile224=
NM_001199984.1:c.883A=	NP_001186913.1:p.Ile295=
NM_005006.6:c.841A=	NP_004997.4:p.Ile281=
XM_017004188.2:c.82A=	XP_016859677.1:p.Ile28=
NM_001199981.2:c.733A=	NP_001186910.1:p.Ile245=
NM_001199982.2:c.508A=	NP_001186911.1:p.Ile170=
NM_001199983.2:c.670A=	NP_001186912.1:p.Ile224=
NM_005006.7:c.841A= MANE Select	NP_004997.4:p.Ile281=
NM_001199984.2:c.883A=	NP_001186913.1:p.Ile295=