Canonical Allele Identifier: CA381541288
Gene: NDUFV1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67611896G>C , CM000673.2:g.67611896G>C GRCh38
NC_000011.9:g.67379367G>C , CM000673.1:g.67379367G>C GRCh37
NC_000011.8:g.67135943G>C NCBI36
NG_013353.1:g.10045G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000322776.11:c.1081-1G>C MANE Select ENSP00000322450.6:n.1081-1G>C
ENST00000647561.1:c.1081-1G>C ENSP00000497587.1:n.1081-1G>C
ENST00000322776.10:c.1081-1G>C ENSP00000322450.6:n.1081-1G>C
ENST00000415352.6:c.1060-1G>C ENSP00000395368.2:n.1060-1G>C
ENST00000526169.1:n.704-1G>C
ENST00000526770.5:n.1364-1G>C
ENST00000527355.5:c.370-224G>C ENSP00000432637.1:n.370-224G>C
ENST00000527923.1:n.423-1G>C
ENST00000529927.5:c.1054-1G>C ENSP00000436766.1:n.1054-1G>C
ENST00000531250.1:n.344G>C
ENST00000532303.5:c.778-1G>C ENSP00000432015.1:n.778-1G>C
ENST00000533919.5:c.485-1G>C ENSP00000435199.1:n.485-1G>C
ENST00000534352.1:n.178G>C
NM_001166102.1:c.1054-1G>C NP_001159574.1:n.1054-1G>C
NM_007103.3:c.1081-1G>C NP_009034.2:n.1081-1G>C
NM_001166102.2:c.1054-1G>C NP_001159574.1:n.1054-1G>C
NM_007103.4:c.1081-1G>C MANE Select NP_009034.2:n.1081-1G>C