Canonical Allele Identifier: CA475412841

Gene: NDUFV1

Linked Data

• MyVariant Identifiers: chr11:g.67378013C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67610542C>A , CM000673.2:g.67610542C>A	GRCh38
NC_000011.9:g.67378013C>A , CM000673.1:g.67378013C>A	GRCh37
NC_000011.8:g.67134589C>A	NCBI36
NG_013353.1:g.8691C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322776.11:c.672C>A MANE Select	ENSP00000322450.6:p.Arg224=
ENST00000647561.1:c.672C>A	ENSP00000497587.1:p.Arg224=
ENST00000322776.10:c.672C>A	ENSP00000322450.6:p.Arg224=
ENST00000415352.6:c.651C>A	ENSP00000395368.2:p.Arg217=
ENST00000526169.1:n.414C>A
ENST00000526770.5:n.531C>A
ENST00000529927.5:c.645C>A	ENSP00000436766.1:p.Arg215=
ENST00000532244.5:c.369C>A	ENSP00000435202.1:p.Arg123=
ENST00000532303.5:c.369C>A	ENSP00000432015.1:p.Arg123=
ENST00000533919.5:c.150C>A	ENSP00000435199.1:p.Arg50=
NM_001166102.1:c.645C>A	NP_001159574.1:p.Arg215=
NM_007103.3:c.672C>A	NP_009034.2:p.Arg224=
NM_001166102.2:c.645C>A	NP_001159574.1:p.Arg215=
NM_007103.4:c.672C>A MANE Select	NP_009034.2:p.Arg224=