Canonical Allele Identifier: CA1980189748

Gene: NDUFV1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67610395G= , CM000673.2:g.67610395G=	GRCh38
NC_000011.9:g.67377866G= , CM000673.1:g.67377866G=	GRCh37
NC_000011.8:g.67134442G=	NCBI36
NG_013353.1:g.8544G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322776.11:c.525G= MANE Select	ENSP00000322450.6:p.Glu175=
ENST00000647561.1:c.525G=	ENSP00000497587.1:p.Glu175=
ENST00000322776.10:c.525G=	ENSP00000322450.6:p.Glu175=
ENST00000415352.6:c.504G=	ENSP00000395368.2:p.Glu168=
ENST00000526169.1:n.267G=
ENST00000526770.5:n.384G=
ENST00000529867.5:c.489G=	ENSP00000434438.1:p.Glu163=
ENST00000529927.5:c.498G=	ENSP00000436766.1:p.Glu166=
ENST00000530638.1:c.408G=	ENSP00000436936.1:p.Glu136=
ENST00000532244.5:c.222G=	ENSP00000435202.1:p.Glu74=
ENST00000532303.5:c.222G=	ENSP00000432015.1:p.Glu74=
ENST00000532343.5:c.222G=	ENSP00000431751.1:p.Glu74=
ENST00000533075.5:c.504G=	ENSP00000437267.1:p.Glu168=
ENST00000533919.5:c.3G=	ENSP00000435199.1:p.Glu1=
NM_001166102.1:c.498G=	NP_001159574.1:p.Glu166=
NM_007103.3:c.525G=	NP_009034.2:p.Glu175=
NM_001166102.2:c.498G=	NP_001159574.1:p.Glu166=
NM_007103.4:c.525G= MANE Select	NP_009034.2:p.Glu175=