Canonical Allele Identifier: CA1980192013
Gene: NDUFV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67611508A= , CM000673.2:g.67611508A= GRCh38
NC_000011.9:g.67378979A= , CM000673.1:g.67378979A= GRCh37
NC_000011.8:g.67135555A= NCBI36
NG_013353.1:g.9657A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000322776.11:c.1019A= MANE Select ENSP00000322450.6:p.Asp340=
ENST00000647561.1:c.1019A= ENSP00000497587.1:p.Asp340=
ENST00000322776.10:c.1019A= ENSP00000322450.6:p.Asp340=
ENST00000415352.6:c.998A= ENSP00000395368.2:p.Asp333=
ENST00000526169.1:n.656-14A=
ENST00000526770.5:n.1302A=
ENST00000527355.5:c.308A= ENSP00000432637.1:p.Asp103=
ENST00000527923.1:n.361A=
ENST00000529927.5:c.992A= ENSP00000436766.1:p.Asp331=
ENST00000532303.5:c.716A= ENSP00000432015.1:p.Asp239=
ENST00000533919.5:c.423A= ENSP00000435199.1:n.423A=
NM_001166102.1:c.992A= NP_001159574.1:p.Asp331=
NM_007103.3:c.1019A= NP_009034.2:p.Asp340=
NM_001166102.2:c.992A= NP_001159574.1:p.Asp331=
NM_007103.4:c.1019A= MANE Select NP_009034.2:p.Asp340=