Canonical Allele Identifier: CA2496487395

Gene: NDUFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.206144982A= , CM000664.2:g.206144982A=	GRCh38
NC_000002.11:g.207009706A= , CM000664.1:g.207009706A=	GRCh37
NC_000002.10:g.206717951A=	NCBI36
NG_009248.1:g.19482T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233190.11:c.782T= MANE Select	ENSP00000233190.5:p.Ile261=
ENST00000233190.10:c.782T=	ENSP00000233190.5:p.Ile261=
ENST00000423725.5:c.611T=	ENSP00000397760.1:p.Ile204=
ENST00000432169.5:c.449T=	ENSP00000409689.1:p.Ile150=
ENST00000440274.5:c.674T=	ENSP00000409766.1:p.Ile225=
ENST00000449699.5:c.782T=	ENSP00000399912.1:p.Ile261=
ENST00000455934.6:c.824T=	ENSP00000392709.2:p.Ile275=
ENST00000457011.5:c.434T=	ENSP00000400976.1:p.Ile145=
NM_001199981.1:c.674T=	NP_001186910.1:p.Ile225=
NM_001199982.1:c.449T=	NP_001186911.1:p.Ile150=
NM_001199983.1:c.611T=	NP_001186912.1:p.Ile204=
NM_001199984.1:c.824T=	NP_001186913.1:p.Ile275=
NM_005006.6:c.782T=	NP_004997.4:p.Ile261=
XM_017004188.2:c.23T=	XP_016859677.1:p.Ile8=
NM_001199981.2:c.674T=	NP_001186910.1:p.Ile225=
NM_001199982.2:c.449T=	NP_001186911.1:p.Ile150=
NM_001199983.2:c.611T=	NP_001186912.1:p.Ile204=
NM_005006.7:c.782T= MANE Select	NP_004997.4:p.Ile261=
NM_001199984.2:c.824T=	NP_001186913.1:p.Ile275=