Canonical Allele Identifier: CA2496487405

Gene: NDUFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.206144999A= , CM000664.2:g.206144999A=	GRCh38
NC_000002.11:g.207009723A= , CM000664.1:g.207009723A=	GRCh37
NC_000002.10:g.206717968A=	NCBI36
NG_009248.1:g.19465T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233190.11:c.765T= MANE Select	ENSP00000233190.5:p.Asp255=
ENST00000233190.10:c.765T=	ENSP00000233190.5:p.Asp255=
ENST00000423725.5:c.594T=	ENSP00000397760.1:p.Asp198=
ENST00000432169.5:c.432T=	ENSP00000409689.1:p.Asp144=
ENST00000440274.5:c.657T=	ENSP00000409766.1:p.Asp219=
ENST00000449699.5:c.765T=	ENSP00000399912.1:p.Asp255=
ENST00000455934.6:c.807T=	ENSP00000392709.2:p.Asp269=
ENST00000457011.5:c.417T=	ENSP00000400976.1:p.Asp139=
NM_001199981.1:c.657T=	NP_001186910.1:p.Asp219=
NM_001199982.1:c.432T=	NP_001186911.1:p.Asp144=
NM_001199983.1:c.594T=	NP_001186912.1:p.Asp198=
NM_001199984.1:c.807T=	NP_001186913.1:p.Asp269=
NM_005006.6:c.765T=	NP_004997.4:p.Asp255=
XM_017004188.2:c.6T=	XP_016859677.1:p.Asp2=
NM_001199981.2:c.657T=	NP_001186910.1:p.Asp219=
NM_001199982.2:c.432T=	NP_001186911.1:p.Asp144=
NM_001199983.2:c.594T=	NP_001186912.1:p.Asp198=
NM_005006.7:c.765T= MANE Select	NP_004997.4:p.Asp255=
NM_001199984.2:c.807T=	NP_001186913.1:p.Asp269=