Canonical Allele Identifier: CA1980192657

Gene: NDUFV1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67611898C= , CM000673.2:g.67611898C=	GRCh38
NC_000011.9:g.67379369C= , CM000673.1:g.67379369C=	GRCh37
NC_000011.8:g.67135945C=	NCBI36
NG_013353.1:g.10047C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000322776.11:c.1082C= MANE Select	ENSP00000322450.6:p.Thr361=
ENST00000647561.1:c.1082C=	ENSP00000497587.1:p.Thr361=
ENST00000322776.10:c.1082C=	ENSP00000322450.6:p.Thr361=
ENST00000415352.6:c.1061C=	ENSP00000395368.2:p.Thr354=
ENST00000526169.1:n.705C=
ENST00000526770.5:n.1365C=
ENST00000527355.5:c.370-222C=	ENSP00000432637.1:n.370-222C=
ENST00000527923.1:n.424C=
ENST00000529927.5:c.1055C=	ENSP00000436766.1:p.Thr352=
ENST00000531250.1:n.346C=
ENST00000532303.5:c.779C=	ENSP00000432015.1:p.Thr260=
ENST00000533919.5:c.486C=	ENSP00000435199.1:n.486C=
ENST00000534352.1:n.180C=
NM_001166102.1:c.1055C=	NP_001159574.1:p.Thr352=
NM_007103.3:c.1082C=	NP_009034.2:p.Thr361=
NM_001166102.2:c.1055C=	NP_001159574.1:p.Thr352=
NM_007103.4:c.1082C= MANE Select	NP_009034.2:p.Thr361=