Canonical Allele Identifier: CA1980189816

Gene: NDUFV1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67610428T= , CM000673.2:g.67610428T=	GRCh38
NC_000011.9:g.67377899T= , CM000673.1:g.67377899T=	GRCh37
NC_000011.8:g.67134475T=	NCBI36
NG_013353.1:g.8577T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322776.11:c.558T= MANE Select	ENSP00000322450.6:p.Ala186=
ENST00000647561.1:c.558T=	ENSP00000497587.1:p.Ala186=
ENST00000322776.10:c.558T=	ENSP00000322450.6:p.Ala186=
ENST00000415352.6:c.537T=	ENSP00000395368.2:p.Ala179=
ENST00000526169.1:n.300T=
ENST00000526770.5:n.417T=
ENST00000529867.5:c.522T=	ENSP00000434438.1:p.Ala174=
ENST00000529927.5:c.531T=	ENSP00000436766.1:p.Ala177=
ENST00000532244.5:c.255T=	ENSP00000435202.1:p.Ala85=
ENST00000532303.5:c.255T=	ENSP00000432015.1:p.Ala85=
ENST00000532343.5:c.255T=	ENSP00000431751.1:p.Ala85=
ENST00000533919.5:c.36T=	ENSP00000435199.1:p.Ala12=
NM_001166102.1:c.531T=	NP_001159574.1:p.Ala177=
NM_007103.3:c.558T=	NP_009034.2:p.Ala186=
NM_001166102.2:c.531T=	NP_001159574.1:p.Ala177=
NM_007103.4:c.558T= MANE Select	NP_009034.2:p.Ala186=