Canonical Allele Identifier: CA1980190062
Gene: NDUFV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67610520A= , CM000673.2:g.67610520A= GRCh38
NC_000011.9:g.67377991A= , CM000673.1:g.67377991A= GRCh37
NC_000011.8:g.67134567A= NCBI36
NG_013353.1:g.8669A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000322776.11:c.650A= MANE Select ENSP00000322450.6:p.Glu217=
ENST00000647561.1:c.650A= ENSP00000497587.1:p.Glu217=
ENST00000322776.10:c.650A= ENSP00000322450.6:p.Glu217=
ENST00000415352.6:c.629A= ENSP00000395368.2:p.Glu210=
ENST00000526169.1:n.392A=
ENST00000526770.5:n.509A=
ENST00000529927.5:c.623A= ENSP00000436766.1:p.Glu208=
ENST00000532244.5:c.347A= ENSP00000435202.1:p.Glu116=
ENST00000532303.5:c.347A= ENSP00000432015.1:p.Glu116=
ENST00000533919.5:c.128A= ENSP00000435199.1:p.Glu43=
NM_001166102.1:c.623A= NP_001159574.1:p.Glu208=
NM_007103.3:c.650A= NP_009034.2:p.Glu217=
NM_001166102.2:c.623A= NP_001159574.1:p.Glu208=
NM_007103.4:c.650A= MANE Select NP_009034.2:p.Glu217=