Canonical Allele Identifier: CA381540923

Gene: NDUFV1

Linked Data

• MyVariant Identifiers: chr11:g.67378975T>G (hg19) ; chr11:g.67611504T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67611504T>G , CM000673.2:g.67611504T>G	GRCh38
NC_000011.9:g.67378975T>G , CM000673.1:g.67378975T>G	GRCh37
NC_000011.8:g.67135551T>G	NCBI36
NG_013353.1:g.9653T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322776.11:c.1015T>G MANE Select	ENSP00000322450.6:p.Phe339Val
ENST00000647561.1:c.1015T>G	ENSP00000497587.1:p.Phe339Val
ENST00000322776.10:c.1015T>G	ENSP00000322450.6:p.Phe339Val
ENST00000415352.6:c.994T>G	ENSP00000395368.2:p.Phe332Val
ENST00000526169.1:n.656-18T>G
ENST00000526770.5:n.1298T>G
ENST00000527355.5:c.304T>G	ENSP00000432637.1:p.Phe102Val
ENST00000527923.1:n.357T>G
ENST00000529927.5:c.988T>G	ENSP00000436766.1:p.Phe330Val
ENST00000532303.5:c.712T>G	ENSP00000432015.1:p.Phe238Val
ENST00000533919.5:c.419T>G	ENSP00000435199.1:n.419T>G
NM_001166102.1:c.988T>G	NP_001159574.1:p.Phe330Val
NM_007103.3:c.1015T>G	NP_009034.2:p.Phe339Val
NM_001166102.2:c.988T>G	NP_001159574.1:p.Phe330Val
NM_007103.4:c.1015T>G MANE Select	NP_009034.2:p.Phe339Val