Canonical Allele Identifier: CA2496487366

Gene: NDUFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.206144920T= , CM000664.2:g.206144920T=	GRCh38
NC_000002.11:g.207009644T= , CM000664.1:g.207009644T=	GRCh37
NC_000002.10:g.206717889T=	NCBI36
NG_009248.1:g.19544A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233190.11:c.844A= MANE Select	ENSP00000233190.5:p.Asn282=
ENST00000233190.10:c.844A=	ENSP00000233190.5:p.Asn282=
ENST00000423725.5:c.673A=	ENSP00000397760.1:p.Asn225=
ENST00000432169.5:c.511A=	ENSP00000409689.1:p.Asn171=
ENST00000440274.5:c.736A=	ENSP00000409766.1:p.Asn246=
ENST00000449699.5:c.844A=	ENSP00000399912.1:p.Asn282=
ENST00000455934.6:c.886A=	ENSP00000392709.2:p.Asn296=
ENST00000457011.5:c.496A=	ENSP00000400976.1:p.Asn166=
NM_001199981.1:c.736A=	NP_001186910.1:p.Asn246=
NM_001199982.1:c.511A=	NP_001186911.1:p.Asn171=
NM_001199983.1:c.673A=	NP_001186912.1:p.Asn225=
NM_001199984.1:c.886A=	NP_001186913.1:p.Asn296=
NM_005006.6:c.844A=	NP_004997.4:p.Asn282=
XM_017004188.2:c.85A=	XP_016859677.1:p.Asn29=
NM_001199981.2:c.736A=	NP_001186910.1:p.Asn246=
NM_001199982.2:c.511A=	NP_001186911.1:p.Asn171=
NM_001199983.2:c.673A=	NP_001186912.1:p.Asn225=
NM_005006.7:c.844A= MANE Select	NP_004997.4:p.Asn282=
NM_001199984.2:c.886A=	NP_001186913.1:p.Asn296=