Canonical Allele Identifier: CA2496487391

Gene: NDUFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.206144970G= , CM000664.2:g.206144970G=	GRCh38
NC_000002.11:g.207009694G= , CM000664.1:g.207009694G=	GRCh37
NC_000002.10:g.206717939G=	NCBI36
NG_009248.1:g.19494C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233190.11:c.794C= MANE Select	ENSP00000233190.5:p.Thr265=
ENST00000233190.10:c.794C=	ENSP00000233190.5:p.Thr265=
ENST00000423725.5:c.623C=	ENSP00000397760.1:p.Thr208=
ENST00000432169.5:c.461C=	ENSP00000409689.1:p.Thr154=
ENST00000440274.5:c.686C=	ENSP00000409766.1:p.Thr229=
ENST00000449699.5:c.794C=	ENSP00000399912.1:p.Thr265=
ENST00000455934.6:c.836C=	ENSP00000392709.2:p.Thr279=
ENST00000457011.5:c.446C=	ENSP00000400976.1:p.Thr149=
NM_001199981.1:c.686C=	NP_001186910.1:p.Thr229=
NM_001199982.1:c.461C=	NP_001186911.1:p.Thr154=
NM_001199983.1:c.623C=	NP_001186912.1:p.Thr208=
NM_001199984.1:c.836C=	NP_001186913.1:p.Thr279=
NM_005006.6:c.794C=	NP_004997.4:p.Thr265=
XM_017004188.2:c.35C=	XP_016859677.1:p.Thr12=
NM_001199981.2:c.686C=	NP_001186910.1:p.Thr229=
NM_001199982.2:c.461C=	NP_001186911.1:p.Thr154=
NM_001199983.2:c.623C=	NP_001186912.1:p.Thr208=
NM_005006.7:c.794C= MANE Select	NP_004997.4:p.Thr265=
NM_001199984.2:c.836C=	NP_001186913.1:p.Thr279=