Canonical Allele Identifier: CA1980189755

Gene: NDUFV1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67610399T= , CM000673.2:g.67610399T=	GRCh38
NC_000011.9:g.67377870T= , CM000673.1:g.67377870T=	GRCh37
NC_000011.8:g.67134446T=	NCBI36
NG_013353.1:g.8548T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322776.11:c.529T= MANE Select	ENSP00000322450.6:p.Tyr177=
ENST00000647561.1:c.529T=	ENSP00000497587.1:p.Tyr177=
ENST00000322776.10:c.529T=	ENSP00000322450.6:p.Tyr177=
ENST00000415352.6:c.508T=	ENSP00000395368.2:p.Tyr170=
ENST00000526169.1:n.271T=
ENST00000526770.5:n.388T=
ENST00000529867.5:c.493T=	ENSP00000434438.1:p.Tyr165=
ENST00000529927.5:c.502T=	ENSP00000436766.1:p.Tyr168=
ENST00000530638.1:c.412T=	ENSP00000436936.1:p.Tyr138=
ENST00000532244.5:c.226T=	ENSP00000435202.1:p.Tyr76=
ENST00000532303.5:c.226T=	ENSP00000432015.1:p.Tyr76=
ENST00000532343.5:c.226T=	ENSP00000431751.1:p.Tyr76=
ENST00000533075.5:c.508T=	ENSP00000437267.1:p.Tyr170=
ENST00000533919.5:c.7T=	ENSP00000435199.1:p.Tyr3=
NM_001166102.1:c.502T=	NP_001159574.1:p.Tyr168=
NM_007103.3:c.529T=	NP_009034.2:p.Tyr177=
NM_001166102.2:c.502T=	NP_001159574.1:p.Tyr168=
NM_007103.4:c.529T= MANE Select	NP_009034.2:p.Tyr177=