Canonical Allele Identifier: CA1980190085
Gene: NDUFV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67610529A= , CM000673.2:g.67610529A= GRCh38
NC_000011.9:g.67378000A= , CM000673.1:g.67378000A= GRCh37
NC_000011.8:g.67134576A= NCBI36
NG_013353.1:g.8678A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000322776.11:c.659A= MANE Select ENSP00000322450.6:p.Gln220=
ENST00000647561.1:c.659A= ENSP00000497587.1:p.Gln220=
ENST00000322776.10:c.659A= ENSP00000322450.6:p.Gln220=
ENST00000415352.6:c.638A= ENSP00000395368.2:p.Gln213=
ENST00000526169.1:n.401A=
ENST00000526770.5:n.518A=
ENST00000529927.5:c.632A= ENSP00000436766.1:p.Gln211=
ENST00000532244.5:c.356A= ENSP00000435202.1:p.Gln119=
ENST00000532303.5:c.356A= ENSP00000432015.1:p.Gln119=
ENST00000533919.5:c.137A= ENSP00000435199.1:p.Gln46=
NM_001166102.1:c.632A= NP_001159574.1:p.Gln211=
NM_007103.3:c.659A= NP_009034.2:p.Gln220=
NM_001166102.2:c.632A= NP_001159574.1:p.Gln211=
NM_007103.4:c.659A= MANE Select NP_009034.2:p.Gln220=