Canonical Allele Identifier: CA2842278199

Gene: NDUFV1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67611849G>A , CM000673.2:g.67611849G>A	GRCh38
NC_000011.9:g.67379320G>A , CM000673.1:g.67379320G>A	GRCh37
NC_000011.8:g.67135896G>A	NCBI36
NG_013353.1:g.9998G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322776.11:c.1081-48G>A MANE Select	ENSP00000322450.6:n.1081-48G>A
ENST00000647561.1:c.1081-48G>A	ENSP00000497587.1:n.1081-48G>A
ENST00000322776.10:c.1081-48G>A	ENSP00000322450.6:n.1081-48G>A
ENST00000415352.6:c.1060-48G>A	ENSP00000395368.2:n.1060-48G>A
ENST00000526169.1:n.704-48G>A
ENST00000526770.5:n.1364-48G>A
ENST00000527355.5:c.370-271G>A	ENSP00000432637.1:n.370-271G>A
ENST00000527923.1:n.423-48G>A
ENST00000529927.5:c.1054-48G>A	ENSP00000436766.1:n.1054-48G>A
ENST00000531250.1:n.297G>A
ENST00000532303.5:c.778-48G>A	ENSP00000432015.1:n.778-48G>A
ENST00000533919.5:c.485-48G>A	ENSP00000435199.1:n.485-48G>A
ENST00000534352.1:n.131G>A
NM_001166102.1:c.1054-48G>A	NP_001159574.1:n.1054-48G>A
NM_007103.3:c.1081-48G>A	NP_009034.2:n.1081-48G>A
NM_001166102.2:c.1054-48G>A	NP_001159574.1:n.1054-48G>A
NM_007103.4:c.1081-48G>A MANE Select	NP_009034.2:n.1081-48G>A