Canonical Allele Identifier: CA1980190198
Gene: NDUFV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67610561G= , CM000673.2:g.67610561G= GRCh38
NC_000011.9:g.67378032G= , CM000673.1:g.67378032G= GRCh37
NC_000011.8:g.67134608G= NCBI36
NG_013353.1:g.8710G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000322776.11:c.691G= MANE Select ENSP00000322450.6:p.Ala231=
ENST00000647561.1:c.691G= ENSP00000497587.1:p.Ala231=
ENST00000322776.10:c.691G= ENSP00000322450.6:p.Ala231=
ENST00000415352.6:c.670G= ENSP00000395368.2:p.Ala224=
ENST00000526169.1:n.433G=
ENST00000526770.5:n.550G=
ENST00000529927.5:c.664G= ENSP00000436766.1:p.Ala222=
ENST00000532244.5:c.388G= ENSP00000435202.1:p.Ala130=
ENST00000532303.5:c.388G= ENSP00000432015.1:p.Ala130=
ENST00000533919.5:c.169G= ENSP00000435199.1:p.Ala57=
NM_001166102.1:c.664G= NP_001159574.1:p.Ala222=
NM_007103.3:c.691G= NP_009034.2:p.Ala231=
NM_001166102.2:c.664G= NP_001159574.1:p.Ala222=
NM_007103.4:c.691G= MANE Select NP_009034.2:p.Ala231=