Canonical Allele Identifier: CA381540607

Gene: NDUFV1

Linked Data

• MyVariant Identifiers: chr11:g.67378916C>G (hg19) ; chr11:g.67611445C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67611445C>G , CM000673.2:g.67611445C>G	GRCh38
NC_000011.9:g.67378916C>G , CM000673.1:g.67378916C>G	GRCh37
NC_000011.8:g.67135492C>G	NCBI36
NG_013353.1:g.9594C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322776.11:c.956C>G MANE Select	ENSP00000322450.6:p.Pro319Arg
ENST00000647561.1:c.956C>G	ENSP00000497587.1:p.Pro319Arg
ENST00000322776.10:c.956C>G	ENSP00000322450.6:p.Pro319Arg
ENST00000415352.6:c.935C>G	ENSP00000395368.2:p.Pro312Arg
ENST00000526169.1:n.656-77C>G
ENST00000526770.5:n.1239C>G
ENST00000527355.5:c.245C>G	ENSP00000432637.1:p.Pro82Arg
ENST00000527923.1:n.298C>G
ENST00000529927.5:c.929C>G	ENSP00000436766.1:p.Pro310Arg
ENST00000532303.5:c.653C>G	ENSP00000432015.1:p.Pro218Arg
ENST00000533919.5:c.392-32C>G	ENSP00000435199.1:n.392-32C>G
NM_001166102.1:c.929C>G	NP_001159574.1:p.Pro310Arg
NM_007103.3:c.956C>G	NP_009034.2:p.Pro319Arg
NM_001166102.2:c.929C>G	NP_001159574.1:p.Pro310Arg
NM_007103.4:c.956C>G MANE Select	NP_009034.2:p.Pro319Arg