Canonical Allele Identifier: CA1980192647
Gene: NDUFV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67611890C= , CM000673.2:g.67611890C= GRCh38
NC_000011.9:g.67379361C= , CM000673.1:g.67379361C= GRCh37
NC_000011.8:g.67135937C= NCBI36
NG_013353.1:g.10039C=

Transcript Alleles

HGVS Amino-acid change
ENST00000322776.11:c.1081-7C= MANE Select ENSP00000322450.6:n.1081-7C=
ENST00000647561.1:c.1081-7C= ENSP00000497587.1:n.1081-7C=
ENST00000322776.10:c.1081-7C= ENSP00000322450.6:n.1081-7C=
ENST00000415352.6:c.1060-7C= ENSP00000395368.2:n.1060-7C=
ENST00000526169.1:n.704-7C=
ENST00000526770.5:n.1364-7C=
ENST00000527355.5:c.370-230C= ENSP00000432637.1:n.370-230C=
ENST00000527923.1:n.423-7C=
ENST00000529927.5:c.1054-7C= ENSP00000436766.1:n.1054-7C=
ENST00000531250.1:n.338C=
ENST00000532303.5:c.778-7C= ENSP00000432015.1:n.778-7C=
ENST00000533919.5:c.485-7C= ENSP00000435199.1:n.485-7C=
ENST00000534352.1:n.172C=
NM_001166102.1:c.1054-7C= NP_001159574.1:n.1054-7C=
NM_007103.3:c.1081-7C= NP_009034.2:n.1081-7C=
NM_001166102.2:c.1054-7C= NP_001159574.1:n.1054-7C=
NM_007103.4:c.1081-7C= MANE Select NP_009034.2:n.1081-7C=