Canonical Allele Identifier: CA1980189859
Gene: NDUFV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67610436C= , CM000673.2:g.67610436C= GRCh38
NC_000011.9:g.67377907C= , CM000673.1:g.67377907C= GRCh37
NC_000011.8:g.67134483C= NCBI36
NG_013353.1:g.8585C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000322776.11:c.566C= MANE Select ENSP00000322450.6:p.Ser189=
ENST00000647561.1:c.566C= ENSP00000497587.1:p.Ser189=
ENST00000322776.10:c.566C= ENSP00000322450.6:p.Ser189=
ENST00000415352.6:c.545C= ENSP00000395368.2:p.Ser182=
ENST00000526169.1:n.308C=
ENST00000526770.5:n.425C=
ENST00000529867.5:c.530C= ENSP00000434438.1:p.Ser177=
ENST00000529927.5:c.539C= ENSP00000436766.1:p.Ser180=
ENST00000532244.5:c.263C= ENSP00000435202.1:p.Ser88=
ENST00000532303.5:c.263C= ENSP00000432015.1:p.Ser88=
ENST00000532343.5:c.263C= ENSP00000431751.1:p.Ser88=
ENST00000533919.5:c.44C= ENSP00000435199.1:p.Ser15=
NM_001166102.1:c.539C= NP_001159574.1:p.Ser180=
NM_007103.3:c.566C= NP_009034.2:p.Ser189=
NM_001166102.2:c.539C= NP_001159574.1:p.Ser180=
NM_007103.4:c.566C= MANE Select NP_009034.2:p.Ser189=