Canonical Allele Identifier: CA381540842

Gene: NDUFV1

Linked Data

• MyVariant Identifiers: chr11:g.67378958A>T (hg19) ; chr11:g.67611487A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67611487A>T , CM000673.2:g.67611487A>T	GRCh38
NC_000011.9:g.67378958A>T , CM000673.1:g.67378958A>T	GRCh37
NC_000011.8:g.67135534A>T	NCBI36
NG_013353.1:g.9636A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322776.11:c.998A>T MANE Select	ENSP00000322450.6:p.Glu333Val
ENST00000647561.1:c.998A>T	ENSP00000497587.1:p.Glu333Val
ENST00000322776.10:c.998A>T	ENSP00000322450.6:p.Glu333Val
ENST00000415352.6:c.977A>T	ENSP00000395368.2:p.Glu326Val
ENST00000526169.1:n.656-35A>T
ENST00000526770.5:n.1281A>T
ENST00000527355.5:c.287A>T	ENSP00000432637.1:p.Glu96Val
ENST00000527923.1:n.340A>T
ENST00000529927.5:c.971A>T	ENSP00000436766.1:p.Glu324Val
ENST00000532303.5:c.695A>T	ENSP00000432015.1:p.Glu232Val
ENST00000533919.5:c.402A>T	ENSP00000435199.1:p.Ter134Cys
NM_001166102.1:c.971A>T	NP_001159574.1:p.Glu324Val
NM_007103.3:c.998A>T	NP_009034.2:p.Glu333Val
NM_001166102.2:c.971A>T	NP_001159574.1:p.Glu324Val
NM_007103.4:c.998A>T MANE Select	NP_009034.2:p.Glu333Val