Canonical Allele Identifier: CA475511049

Gene: NDUFV1

Linked Data

• MyVariant Identifiers: chr11:g.67379427C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67611956C>A , CM000673.2:g.67611956C>A	GRCh38
NC_000011.9:g.67379427C>A , CM000673.1:g.67379427C>A	GRCh37
NC_000011.8:g.67136003C>A	NCBI36
NG_013353.1:g.10105C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322776.11:c.1140C>A MANE Select	ENSP00000322450.6:p.Gly380=
ENST00000647561.1:c.1140C>A	ENSP00000497587.1:p.Gly380=
ENST00000322776.10:c.1140C>A	ENSP00000322450.6:p.Gly380=
ENST00000415352.6:c.1119C>A	ENSP00000395368.2:p.Gly373=
ENST00000526169.1:n.763C>A
ENST00000526770.5:n.1423C>A
ENST00000527355.5:c.370-164C>A	ENSP00000432637.1:n.370-164C>A
ENST00000527923.1:n.482C>A
ENST00000529927.5:c.1113C>A	ENSP00000436766.1:p.Gly371=
ENST00000531250.1:n.404C>A
ENST00000532303.5:c.837C>A	ENSP00000432015.1:p.Gly279=
ENST00000533919.5:c.544C>A	ENSP00000435199.1:n.544C>A
ENST00000534352.1:n.238C>A
NM_001166102.1:c.1113C>A	NP_001159574.1:p.Gly371=
NM_007103.3:c.1140C>A	NP_009034.2:p.Gly380=
NM_001166102.2:c.1113C>A	NP_001159574.1:p.Gly371=
NM_007103.4:c.1140C>A MANE Select	NP_009034.2:p.Gly380=