Canonical Allele Identifier: CA2496479100

Gene: NDUFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.206127856C= , CM000664.2:g.206127856C=	GRCh38
NC_000002.11:g.206992580C= , CM000664.1:g.206992580C=	GRCh37
NC_000002.10:g.206700825C=	NCBI36
NG_009248.1:g.36608G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233190.11:c.1825G= MANE Select	ENSP00000233190.5:p.Ala609=
ENST00000233190.10:c.1825G=	ENSP00000233190.5:p.Ala609=
ENST00000423725.5:c.1654G=	ENSP00000397760.1:p.Ala552=
ENST00000432169.5:c.1492G=	ENSP00000409689.1:p.Ala498=
ENST00000440274.5:c.1717G=	ENSP00000409766.1:p.Ala573=
ENST00000449699.5:c.1825G=	ENSP00000399912.1:p.Ala609=
ENST00000455934.6:c.1867G=	ENSP00000392709.2:p.Ala623=
ENST00000457011.5:c.1477G=	ENSP00000400976.1:p.Ala493=
ENST00000498520.1:n.297G=
NM_001199981.1:c.1717G=	NP_001186910.1:p.Ala573=
NM_001199982.1:c.1492G=	NP_001186911.1:p.Ala498=
NM_001199983.1:c.1654G=	NP_001186912.1:p.Ala552=
NM_001199984.1:c.1867G=	NP_001186913.1:p.Ala623=
NM_005006.6:c.1825G=	NP_004997.4:p.Ala609=
XM_017004188.2:c.1066G=	XP_016859677.1:p.Ala356=
NM_001199981.2:c.1717G=	NP_001186910.1:p.Ala573=
NM_001199982.2:c.1492G=	NP_001186911.1:p.Ala498=
NM_001199983.2:c.1654G=	NP_001186912.1:p.Ala552=
NM_005006.7:c.1825G= MANE Select	NP_004997.4:p.Ala609=
NM_001199984.2:c.1867G=	NP_001186913.1:p.Ala623=