Canonical Allele Identifier: CA1980192637
Gene: NDUFV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67611887C= , CM000673.2:g.67611887C= GRCh38
NC_000011.9:g.67379358C= , CM000673.1:g.67379358C= GRCh37
NC_000011.8:g.67135934C= NCBI36
NG_013353.1:g.10036C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000322776.11:c.1081-10C= MANE Select ENSP00000322450.6:n.1081-10C=
ENST00000647561.1:c.1081-10C= ENSP00000497587.1:n.1081-10C=
ENST00000322776.10:c.1081-10C= ENSP00000322450.6:n.1081-10C=
ENST00000415352.6:c.1060-10C= ENSP00000395368.2:n.1060-10C=
ENST00000526169.1:n.704-10C=
ENST00000526770.5:n.1364-10C=
ENST00000527355.5:c.370-233C= ENSP00000432637.1:n.370-233C=
ENST00000527923.1:n.423-10C=
ENST00000529927.5:c.1054-10C= ENSP00000436766.1:n.1054-10C=
ENST00000531250.1:n.335C=
ENST00000532303.5:c.778-10C= ENSP00000432015.1:n.778-10C=
ENST00000533919.5:c.485-10C= ENSP00000435199.1:n.485-10C=
ENST00000534352.1:n.169C=
NM_001166102.1:c.1054-10C= NP_001159574.1:n.1054-10C=
NM_007103.3:c.1081-10C= NP_009034.2:n.1081-10C=
NM_001166102.2:c.1054-10C= NP_001159574.1:n.1054-10C=
NM_007103.4:c.1081-10C= MANE Select NP_009034.2:n.1081-10C=