Canonical Allele Identifier: CA2496479147

Gene: NDUFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.206127964C= , CM000664.2:g.206127964C=	GRCh38
NC_000002.11:g.206992688C= , CM000664.1:g.206992688C=	GRCh37
NC_000002.10:g.206700933C=	NCBI36
NG_009248.1:g.36500G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233190.11:c.1717G= MANE Select	ENSP00000233190.5:p.Gly573=
ENST00000233190.10:c.1717G=	ENSP00000233190.5:p.Gly573=
ENST00000423725.5:c.1546G=	ENSP00000397760.1:p.Gly516=
ENST00000432169.5:c.1384G=	ENSP00000409689.1:p.Gly462=
ENST00000440274.5:c.1609G=	ENSP00000409766.1:p.Gly537=
ENST00000449699.5:c.1717G=	ENSP00000399912.1:p.Gly573=
ENST00000455934.6:c.1759G=	ENSP00000392709.2:p.Gly587=
ENST00000457011.5:c.1369G=	ENSP00000400976.1:p.Gly457=
ENST00000498520.1:n.189G=
NM_001199981.1:c.1609G=	NP_001186910.1:p.Gly537=
NM_001199982.1:c.1384G=	NP_001186911.1:p.Gly462=
NM_001199983.1:c.1546G=	NP_001186912.1:p.Gly516=
NM_001199984.1:c.1759G=	NP_001186913.1:p.Gly587=
NM_005006.6:c.1717G=	NP_004997.4:p.Gly573=
XM_017004188.2:c.958G=	XP_016859677.1:p.Gly320=
NM_001199981.2:c.1609G=	NP_001186910.1:p.Gly537=
NM_001199982.2:c.1384G=	NP_001186911.1:p.Gly462=
NM_001199983.2:c.1546G=	NP_001186912.1:p.Gly516=
NM_005006.7:c.1717G= MANE Select	NP_004997.4:p.Gly573=
NM_001199984.2:c.1759G=	NP_001186913.1:p.Gly587=