Canonical Allele Identifier: CA1980191940
Gene: NDUFV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67611489A= , CM000673.2:g.67611489A= GRCh38
NC_000011.9:g.67378960A= , CM000673.1:g.67378960A= GRCh37
NC_000011.8:g.67135536A= NCBI36
NG_013353.1:g.9638A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000322776.11:c.1000A= MANE Select ENSP00000322450.6:p.Thr334=
ENST00000647561.1:c.1000A= ENSP00000497587.1:p.Thr334=
ENST00000322776.10:c.1000A= ENSP00000322450.6:p.Thr334=
ENST00000415352.6:c.979A= ENSP00000395368.2:p.Thr327=
ENST00000526169.1:n.656-33A=
ENST00000526770.5:n.1283A=
ENST00000527355.5:c.289A= ENSP00000432637.1:p.Thr97=
ENST00000527923.1:n.342A=
ENST00000529927.5:c.973A= ENSP00000436766.1:p.Thr325=
ENST00000532303.5:c.697A= ENSP00000432015.1:p.Thr233=
ENST00000533919.5:c.404A= ENSP00000435199.1:n.404A=
NM_001166102.1:c.973A= NP_001159574.1:p.Thr325=
NM_007103.3:c.1000A= NP_009034.2:p.Thr334=
NM_001166102.2:c.973A= NP_001159574.1:p.Thr325=
NM_007103.4:c.1000A= MANE Select NP_009034.2:p.Thr334=