Canonical Allele Identifier: CA2496479140

Gene: NDUFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.206127950A= , CM000664.2:g.206127950A=	GRCh38
NC_000002.11:g.206992674A= , CM000664.1:g.206992674A=	GRCh37
NC_000002.10:g.206700919A=	NCBI36
NG_009248.1:g.36514T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233190.11:c.1731T= MANE Select	ENSP00000233190.5:p.Ala577=
ENST00000233190.10:c.1731T=	ENSP00000233190.5:p.Ala577=
ENST00000423725.5:c.1560T=	ENSP00000397760.1:p.Ala520=
ENST00000432169.5:c.1398T=	ENSP00000409689.1:p.Ala466=
ENST00000440274.5:c.1623T=	ENSP00000409766.1:p.Ala541=
ENST00000449699.5:c.1731T=	ENSP00000399912.1:p.Ala577=
ENST00000455934.6:c.1773T=	ENSP00000392709.2:p.Ala591=
ENST00000457011.5:c.1383T=	ENSP00000400976.1:p.Ala461=
ENST00000498520.1:n.203T=
NM_001199981.1:c.1623T=	NP_001186910.1:p.Ala541=
NM_001199982.1:c.1398T=	NP_001186911.1:p.Ala466=
NM_001199983.1:c.1560T=	NP_001186912.1:p.Ala520=
NM_001199984.1:c.1773T=	NP_001186913.1:p.Ala591=
NM_005006.6:c.1731T=	NP_004997.4:p.Ala577=
XM_017004188.2:c.972T=	XP_016859677.1:p.Ala324=
NM_001199981.2:c.1623T=	NP_001186910.1:p.Ala541=
NM_001199982.2:c.1398T=	NP_001186911.1:p.Ala466=
NM_001199983.2:c.1560T=	NP_001186912.1:p.Ala520=
NM_005006.7:c.1731T= MANE Select	NP_004997.4:p.Ala577=
NM_001199984.2:c.1773T=	NP_001186913.1:p.Ala591=