Canonical Allele Identifier: CA2496487387

Gene: NDUFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.206144965T= , CM000664.2:g.206144965T=	GRCh38
NC_000002.11:g.207009689T= , CM000664.1:g.207009689T=	GRCh37
NC_000002.10:g.206717934T=	NCBI36
NG_009248.1:g.19499A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233190.11:c.799A= MANE Select	ENSP00000233190.5:p.Thr267=
ENST00000233190.10:c.799A=	ENSP00000233190.5:p.Thr267=
ENST00000423725.5:c.628A=	ENSP00000397760.1:p.Thr210=
ENST00000432169.5:c.466A=	ENSP00000409689.1:p.Thr156=
ENST00000440274.5:c.691A=	ENSP00000409766.1:p.Thr231=
ENST00000449699.5:c.799A=	ENSP00000399912.1:p.Thr267=
ENST00000455934.6:c.841A=	ENSP00000392709.2:p.Thr281=
ENST00000457011.5:c.451A=	ENSP00000400976.1:p.Thr151=
NM_001199981.1:c.691A=	NP_001186910.1:p.Thr231=
NM_001199982.1:c.466A=	NP_001186911.1:p.Thr156=
NM_001199983.1:c.628A=	NP_001186912.1:p.Thr210=
NM_001199984.1:c.841A=	NP_001186913.1:p.Thr281=
NM_005006.6:c.799A=	NP_004997.4:p.Thr267=
XM_017004188.2:c.40A=	XP_016859677.1:p.Thr14=
NM_001199981.2:c.691A=	NP_001186910.1:p.Thr231=
NM_001199982.2:c.466A=	NP_001186911.1:p.Thr156=
NM_001199983.2:c.628A=	NP_001186912.1:p.Thr210=
NM_005006.7:c.799A= MANE Select	NP_004997.4:p.Thr267=
NM_001199984.2:c.841A=	NP_001186913.1:p.Thr281=