Canonical Allele Identifier: CA475511022

Gene: NDUFV1

Linked Data

• MyVariant Identifiers: chr11:g.67379382A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67611911A>G , CM000673.2:g.67611911A>G	GRCh38
NC_000011.9:g.67379382A>G , CM000673.1:g.67379382A>G	GRCh37
NC_000011.8:g.67135958A>G	NCBI36
NG_013353.1:g.10060A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322776.11:c.1095A>G MANE Select	ENSP00000322450.6:p.Lys365=
ENST00000647561.1:c.1095A>G	ENSP00000497587.1:p.Lys365=
ENST00000322776.10:c.1095A>G	ENSP00000322450.6:p.Lys365=
ENST00000415352.6:c.1074A>G	ENSP00000395368.2:p.Lys358=
ENST00000526169.1:n.718A>G
ENST00000526770.5:n.1378A>G
ENST00000527355.5:c.370-209A>G	ENSP00000432637.1:n.370-209A>G
ENST00000527923.1:n.437A>G
ENST00000529927.5:c.1068A>G	ENSP00000436766.1:p.Lys356=
ENST00000531250.1:n.359A>G
ENST00000532303.5:c.792A>G	ENSP00000432015.1:p.Lys264=
ENST00000533919.5:c.499A>G	ENSP00000435199.1:n.499A>G
ENST00000534352.1:n.193A>G
NM_001166102.1:c.1068A>G	NP_001159574.1:p.Lys356=
NM_007103.3:c.1095A>G	NP_009034.2:p.Lys365=
NM_001166102.2:c.1068A>G	NP_001159574.1:p.Lys356=
NM_007103.4:c.1095A>G MANE Select	NP_009034.2:p.Lys365=