Canonical Allele Identifier: CA1980191859
Gene: NDUFV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67611475A= , CM000673.2:g.67611475A= GRCh38
NC_000011.9:g.67378946A= , CM000673.1:g.67378946A= GRCh37
NC_000011.8:g.67135522A= NCBI36
NG_013353.1:g.9624A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000322776.11:c.986A= MANE Select ENSP00000322450.6:p.Lys329=
ENST00000647561.1:c.986A= ENSP00000497587.1:p.Lys329=
ENST00000322776.10:c.986A= ENSP00000322450.6:p.Lys329=
ENST00000415352.6:c.965A= ENSP00000395368.2:p.Lys322=
ENST00000526169.1:n.656-47A=
ENST00000526770.5:n.1269A=
ENST00000527355.5:c.275A= ENSP00000432637.1:p.Lys92=
ENST00000527923.1:n.328A=
ENST00000529927.5:c.959A= ENSP00000436766.1:p.Lys320=
ENST00000532303.5:c.683A= ENSP00000432015.1:p.Lys228=
ENST00000533919.5:c.392-2A= ENSP00000435199.1:n.392-2A=
NM_001166102.1:c.959A= NP_001159574.1:p.Lys320=
NM_007103.3:c.986A= NP_009034.2:p.Lys329=
NM_001166102.2:c.959A= NP_001159574.1:p.Lys320=
NM_007103.4:c.986A= MANE Select NP_009034.2:p.Lys329=