Canonical Allele Identifier: CA2496487403

Gene: NDUFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.206144997G= , CM000664.2:g.206144997G=	GRCh38
NC_000002.11:g.207009721G= , CM000664.1:g.207009721G=	GRCh37
NC_000002.10:g.206717966G=	NCBI36
NG_009248.1:g.19467C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233190.11:c.767C= MANE Select	ENSP00000233190.5:p.Ala256=
ENST00000233190.10:c.767C=	ENSP00000233190.5:p.Ala256=
ENST00000423725.5:c.596C=	ENSP00000397760.1:p.Ala199=
ENST00000432169.5:c.434C=	ENSP00000409689.1:p.Ala145=
ENST00000440274.5:c.659C=	ENSP00000409766.1:p.Ala220=
ENST00000449699.5:c.767C=	ENSP00000399912.1:p.Ala256=
ENST00000455934.6:c.809C=	ENSP00000392709.2:p.Ala270=
ENST00000457011.5:c.419C=	ENSP00000400976.1:p.Ala140=
NM_001199981.1:c.659C=	NP_001186910.1:p.Ala220=
NM_001199982.1:c.434C=	NP_001186911.1:p.Ala145=
NM_001199983.1:c.596C=	NP_001186912.1:p.Ala199=
NM_001199984.1:c.809C=	NP_001186913.1:p.Ala270=
NM_005006.6:c.767C=	NP_004997.4:p.Ala256=
XM_017004188.2:c.8C=	XP_016859677.1:p.Ala3=
NM_001199981.2:c.659C=	NP_001186910.1:p.Ala220=
NM_001199982.2:c.434C=	NP_001186911.1:p.Ala145=
NM_001199983.2:c.596C=	NP_001186912.1:p.Ala199=
NM_005006.7:c.767C= MANE Select	NP_004997.4:p.Ala256=
NM_001199984.2:c.809C=	NP_001186913.1:p.Ala270=