Canonical Allele Identifier: CA1980192394

Gene: NDUFV1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67611706G= , CM000673.2:g.67611706G=	GRCh38
NC_000011.9:g.67379177G= , CM000673.1:g.67379177G=	GRCh37
NC_000011.8:g.67135753G=	NCBI36
NG_013353.1:g.9855G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322776.11:c.1080+137G= MANE Select	ENSP00000322450.6:n.1080+137G=
ENST00000647561.1:c.1080+137G=	ENSP00000497587.1:n.1080+137G=
ENST00000322776.10:c.1080+137G=	ENSP00000322450.6:n.1080+137G=
ENST00000415352.6:c.1059+137G=	ENSP00000395368.2:n.1059+137G=
ENST00000526169.1:n.703+137G=
ENST00000526770.5:n.1363+137G=
ENST00000527355.5:c.369+137G=	ENSP00000432637.1:n.369+137G=
ENST00000527923.1:n.422+137G=
ENST00000529927.5:c.1053+137G=	ENSP00000436766.1:n.1053+137G=
ENST00000531250.1:n.154G=
ENST00000532303.5:c.777+137G=	ENSP00000432015.1:n.777+137G=
ENST00000533919.5:c.484+137G=	ENSP00000435199.1:n.484+137G=
NM_001166102.1:c.1053+137G=	NP_001159574.1:n.1053+137G=
NM_007103.3:c.1080+137G=	NP_009034.2:n.1080+137G=
NM_001166102.2:c.1053+137G=	NP_001159574.1:n.1053+137G=
NM_007103.4:c.1080+137G= MANE Select	NP_009034.2:n.1080+137G=