Canonical Allele Identifier: CA1980190039
Gene: NDUFV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67610515C= , CM000673.2:g.67610515C= GRCh38
NC_000011.9:g.67377986C= , CM000673.1:g.67377986C= GRCh37
NC_000011.8:g.67134562C= NCBI36
NG_013353.1:g.8664C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000322776.11:c.645C= MANE Select ENSP00000322450.6:p.Ser215=
ENST00000647561.1:c.645C= ENSP00000497587.1:p.Ser215=
ENST00000322776.10:c.645C= ENSP00000322450.6:p.Ser215=
ENST00000415352.6:c.624C= ENSP00000395368.2:p.Ser208=
ENST00000526169.1:n.387C=
ENST00000526770.5:n.504C=
ENST00000529927.5:c.618C= ENSP00000436766.1:p.Ser206=
ENST00000532244.5:c.342C= ENSP00000435202.1:p.Ser114=
ENST00000532303.5:c.342C= ENSP00000432015.1:p.Ser114=
ENST00000533919.5:c.123C= ENSP00000435199.1:p.Ser41=
NM_001166102.1:c.618C= NP_001159574.1:p.Ser206=
NM_007103.3:c.645C= NP_009034.2:p.Ser215=
NM_001166102.2:c.618C= NP_001159574.1:p.Ser206=
NM_007103.4:c.645C= MANE Select NP_009034.2:p.Ser215=