Canonical Allele Identifier: CA1980191960
Gene: NDUFV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67611492G= , CM000673.2:g.67611492G= GRCh38
NC_000011.9:g.67378963G= , CM000673.1:g.67378963G= GRCh37
NC_000011.8:g.67135539G= NCBI36
NG_013353.1:g.9641G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000322776.11:c.1003G= MANE Select ENSP00000322450.6:p.Val335=
ENST00000647561.1:c.1003G= ENSP00000497587.1:p.Val335=
ENST00000322776.10:c.1003G= ENSP00000322450.6:p.Val335=
ENST00000415352.6:c.982G= ENSP00000395368.2:p.Val328=
ENST00000526169.1:n.656-30G=
ENST00000526770.5:n.1286G=
ENST00000527355.5:c.292G= ENSP00000432637.1:p.Val98=
ENST00000527923.1:n.345G=
ENST00000529927.5:c.976G= ENSP00000436766.1:p.Val326=
ENST00000532303.5:c.700G= ENSP00000432015.1:p.Val234=
ENST00000533919.5:c.407G= ENSP00000435199.1:n.407G=
NM_001166102.1:c.976G= NP_001159574.1:p.Val326=
NM_007103.3:c.1003G= NP_009034.2:p.Val335=
NM_001166102.2:c.976G= NP_001159574.1:p.Val326=
NM_007103.4:c.1003G= MANE Select NP_009034.2:p.Val335=