Canonical Allele Identifier: CA1980191792
Gene: NDUFV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67611451G= , CM000673.2:g.67611451G= GRCh38
NC_000011.9:g.67378922G= , CM000673.1:g.67378922G= GRCh37
NC_000011.8:g.67135498G= NCBI36
NG_013353.1:g.9600G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000322776.11:c.962G= MANE Select ENSP00000322450.6:p.Gly321=
ENST00000647561.1:c.962G= ENSP00000497587.1:p.Gly321=
ENST00000322776.10:c.962G= ENSP00000322450.6:p.Gly321=
ENST00000415352.6:c.941G= ENSP00000395368.2:p.Gly314=
ENST00000526169.1:n.656-71G=
ENST00000526770.5:n.1245G=
ENST00000527355.5:c.251G= ENSP00000432637.1:p.Gly84=
ENST00000527923.1:n.304G=
ENST00000529927.5:c.935G= ENSP00000436766.1:p.Gly312=
ENST00000532303.5:c.659G= ENSP00000432015.1:p.Gly220=
ENST00000533919.5:c.392-26G= ENSP00000435199.1:n.392-26G=
NM_001166102.1:c.935G= NP_001159574.1:p.Gly312=
NM_007103.3:c.962G= NP_009034.2:p.Gly321=
NM_001166102.2:c.935G= NP_001159574.1:p.Gly312=
NM_007103.4:c.962G= MANE Select NP_009034.2:p.Gly321=