Canonical Allele Identifier: CA2496479119

Gene: NDUFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.206127909T= , CM000664.2:g.206127909T=	GRCh38
NC_000002.11:g.206992633T= , CM000664.1:g.206992633T=	GRCh37
NC_000002.10:g.206700878T=	NCBI36
NG_009248.1:g.36555A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233190.11:c.1772A= MANE Select	ENSP00000233190.5:p.Glu591=
ENST00000233190.10:c.1772A=	ENSP00000233190.5:p.Glu591=
ENST00000423725.5:c.1601A=	ENSP00000397760.1:p.Glu534=
ENST00000432169.5:c.1439A=	ENSP00000409689.1:p.Glu480=
ENST00000440274.5:c.1664A=	ENSP00000409766.1:p.Glu555=
ENST00000449699.5:c.1772A=	ENSP00000399912.1:p.Glu591=
ENST00000455934.6:c.1814A=	ENSP00000392709.2:p.Glu605=
ENST00000457011.5:c.1424A=	ENSP00000400976.1:p.Glu475=
ENST00000498520.1:n.244A=
NM_001199981.1:c.1664A=	NP_001186910.1:p.Glu555=
NM_001199982.1:c.1439A=	NP_001186911.1:p.Glu480=
NM_001199983.1:c.1601A=	NP_001186912.1:p.Glu534=
NM_001199984.1:c.1814A=	NP_001186913.1:p.Glu605=
NM_005006.6:c.1772A=	NP_004997.4:p.Glu591=
XM_017004188.2:c.1013A=	XP_016859677.1:p.Glu338=
NM_001199981.2:c.1664A=	NP_001186910.1:p.Glu555=
NM_001199982.2:c.1439A=	NP_001186911.1:p.Glu480=
NM_001199983.2:c.1601A=	NP_001186912.1:p.Glu534=
NM_005006.7:c.1772A= MANE Select	NP_004997.4:p.Glu591=
NM_001199984.2:c.1814A=	NP_001186913.1:p.Glu605=