Canonical Allele Identifier: CA1980188259

Gene: NDUFV1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67609479C= , CM000673.2:g.67609479C=	GRCh38
NC_000011.9:g.67376950C= , CM000673.1:g.67376950C=	GRCh37
NC_000011.8:g.67133526C=	NCBI36
NG_013353.1:g.7628C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322776.11:c.354C= MANE Select	ENSP00000322450.6:p.Asp118=
ENST00000647561.1:c.354C=	ENSP00000497587.1:p.Asp118=
ENST00000322776.10:c.354C=	ENSP00000322450.6:p.Asp118=
ENST00000415352.6:c.333C=	ENSP00000395368.2:p.Asp111=
ENST00000524838.5:n.411C=
ENST00000525086.5:n.427C=
ENST00000526169.1:n.96C=
ENST00000526770.5:n.213C=
ENST00000528314.1:c.51C=	ENSP00000434581.1:p.Asp17=
ENST00000528377.1:n.525C=
ENST00000529867.5:c.318C=	ENSP00000434438.1:p.Asp106=
ENST00000529927.5:c.327C=	ENSP00000436766.1:p.Asp109=
ENST00000530014.5:n.649C=
ENST00000530103.5:c.*248C=	ENSP00000434575.1:n.*248C=
ENST00000530638.1:c.237C=	ENSP00000436936.1:p.Asp79=
ENST00000532244.5:c.51C=	ENSP00000435202.1:p.Asp17=
ENST00000532303.5:c.51C=	ENSP00000432015.1:p.Asp17=
ENST00000532343.5:c.51C=	ENSP00000431751.1:p.Asp17=
ENST00000533075.5:c.333C=	ENSP00000437267.1:p.Asp111=
ENST00000534139.5:n.470C=
NM_001166102.1:c.327C=	NP_001159574.1:p.Asp109=
NM_007103.3:c.354C=	NP_009034.2:p.Asp118=
NM_001166102.2:c.327C=	NP_001159574.1:p.Asp109=
NM_007103.4:c.354C= MANE Select	NP_009034.2:p.Asp118=