Canonical Allele Identifier: CA1980188282

Gene: NDUFV1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67609484G= , CM000673.2:g.67609484G=	GRCh38
NC_000011.9:g.67376955G= , CM000673.1:g.67376955G=	GRCh37
NC_000011.8:g.67133531G=	NCBI36
NG_013353.1:g.7633G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322776.11:c.359G= MANE Select	ENSP00000322450.6:p.Gly120=
ENST00000647561.1:c.359G=	ENSP00000497587.1:p.Gly120=
ENST00000322776.10:c.359G=	ENSP00000322450.6:p.Gly120=
ENST00000415352.6:c.338G=	ENSP00000395368.2:p.Gly113=
ENST00000524838.5:n.416G=
ENST00000525086.5:n.432G=
ENST00000526169.1:n.101G=
ENST00000526770.5:n.218G=
ENST00000528314.1:c.56G=	ENSP00000434581.1:p.Gly19=
ENST00000528377.1:n.530G=
ENST00000529867.5:c.323G=	ENSP00000434438.1:p.Gly108=
ENST00000529927.5:c.332G=	ENSP00000436766.1:p.Gly111=
ENST00000530014.5:n.654G=
ENST00000530103.5:c.*253G=	ENSP00000434575.1:n.*253G=
ENST00000530638.1:c.242G=	ENSP00000436936.1:p.Gly81=
ENST00000532244.5:c.56G=	ENSP00000435202.1:p.Gly19=
ENST00000532303.5:c.56G=	ENSP00000432015.1:p.Gly19=
ENST00000532343.5:c.56G=	ENSP00000431751.1:p.Gly19=
ENST00000533075.5:c.338G=	ENSP00000437267.1:p.Gly113=
ENST00000534139.5:n.475G=
NM_001166102.1:c.332G=	NP_001159574.1:p.Gly111=
NM_007103.3:c.359G=	NP_009034.2:p.Gly120=
NM_001166102.2:c.332G=	NP_001159574.1:p.Gly111=
NM_007103.4:c.359G= MANE Select	NP_009034.2:p.Gly120=