Canonical Allele Identifier: CA2792509547

Gene: NDUFV1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67611865T>G , CM000673.2:g.67611865T>G	GRCh38
NC_000011.9:g.67379336T>G , CM000673.1:g.67379336T>G	GRCh37
NC_000011.8:g.67135912T>G	NCBI36
NG_013353.1:g.10014T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322776.11:c.1081-32T>G MANE Select	ENSP00000322450.6:n.1081-32T>G
ENST00000647561.1:c.1081-32T>G	ENSP00000497587.1:n.1081-32T>G
ENST00000322776.10:c.1081-32T>G	ENSP00000322450.6:n.1081-32T>G
ENST00000415352.6:c.1060-32T>G	ENSP00000395368.2:n.1060-32T>G
ENST00000526169.1:n.704-32T>G
ENST00000526770.5:n.1364-32T>G
ENST00000527355.5:c.370-255T>G	ENSP00000432637.1:n.370-255T>G
ENST00000527923.1:n.423-32T>G
ENST00000529927.5:c.1054-32T>G	ENSP00000436766.1:n.1054-32T>G
ENST00000531250.1:n.313T>G
ENST00000532303.5:c.778-32T>G	ENSP00000432015.1:n.778-32T>G
ENST00000533919.5:c.485-32T>G	ENSP00000435199.1:n.485-32T>G
ENST00000534352.1:n.147T>G
NM_001166102.1:c.1054-32T>G	NP_001159574.1:n.1054-32T>G
NM_007103.3:c.1081-32T>G	NP_009034.2:n.1081-32T>G
NM_001166102.2:c.1054-32T>G	NP_001159574.1:n.1054-32T>G
NM_007103.4:c.1081-32T>G MANE Select	NP_009034.2:n.1081-32T>G