Canonical Allele Identifier: CA475511062

Gene: NDUFV1

Linked Data

• MyVariant Identifiers: chr11:g.67379445T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67611974T>A , CM000673.2:g.67611974T>A	GRCh38
NC_000011.9:g.67379445T>A , CM000673.1:g.67379445T>A	GRCh37
NC_000011.8:g.67136021T>A	NCBI36
NG_013353.1:g.10123T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322776.11:c.1158T>A MANE Select	ENSP00000322450.6:p.Arg386=
ENST00000647561.1:c.1158T>A	ENSP00000497587.1:p.Arg386=
ENST00000322776.10:c.1158T>A	ENSP00000322450.6:p.Arg386=
ENST00000415352.6:c.1137T>A	ENSP00000395368.2:p.Arg379=
ENST00000526770.5:n.1441T>A
ENST00000527355.5:c.370-146T>A	ENSP00000432637.1:n.370-146T>A
ENST00000527923.1:n.500T>A
ENST00000529927.5:c.1131T>A	ENSP00000436766.1:p.Arg377=
ENST00000531250.1:n.422T>A
ENST00000532303.5:c.855T>A	ENSP00000432015.1:p.Arg285=
ENST00000533919.5:c.562T>A	ENSP00000435199.1:n.562T>A
ENST00000534352.1:n.256T>A
NM_001166102.1:c.1131T>A	NP_001159574.1:p.Arg377=
NM_007103.3:c.1158T>A	NP_009034.2:p.Arg386=
NM_001166102.2:c.1131T>A	NP_001159574.1:p.Arg377=
NM_007103.4:c.1158T>A MANE Select	NP_009034.2:p.Arg386=