Canonical Allele Identifier: CA2496487372

Gene: NDUFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.206144934A= , CM000664.2:g.206144934A=	GRCh38
NC_000002.11:g.207009658A= , CM000664.1:g.207009658A=	GRCh37
NC_000002.10:g.206717903A=	NCBI36
NG_009248.1:g.19530T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233190.11:c.830T= MANE Select	ENSP00000233190.5:p.Met277=
ENST00000233190.10:c.830T=	ENSP00000233190.5:p.Met277=
ENST00000423725.5:c.659T=	ENSP00000397760.1:p.Met220=
ENST00000432169.5:c.497T=	ENSP00000409689.1:p.Met166=
ENST00000440274.5:c.722T=	ENSP00000409766.1:p.Met241=
ENST00000449699.5:c.830T=	ENSP00000399912.1:p.Met277=
ENST00000455934.6:c.872T=	ENSP00000392709.2:p.Met291=
ENST00000457011.5:c.482T=	ENSP00000400976.1:p.Met161=
NM_001199981.1:c.722T=	NP_001186910.1:p.Met241=
NM_001199982.1:c.497T=	NP_001186911.1:p.Met166=
NM_001199983.1:c.659T=	NP_001186912.1:p.Met220=
NM_001199984.1:c.872T=	NP_001186913.1:p.Met291=
NM_005006.6:c.830T=	NP_004997.4:p.Met277=
XM_017004188.2:c.71T=	XP_016859677.1:p.Met24=
NM_001199981.2:c.722T=	NP_001186910.1:p.Met241=
NM_001199982.2:c.497T=	NP_001186911.1:p.Met166=
NM_001199983.2:c.659T=	NP_001186912.1:p.Met220=
NM_005006.7:c.830T= MANE Select	NP_004997.4:p.Met277=
NM_001199984.2:c.872T=	NP_001186913.1:p.Met291=