Canonical Allele Identifier: CA1980192960

Gene: NDUFV1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67611996T= , CM000673.2:g.67611996T=	GRCh38
NC_000011.9:g.67379467T= , CM000673.1:g.67379467T=	GRCh37
NC_000011.8:g.67136043T=	NCBI36
NG_013353.1:g.10145T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322776.11:c.1162+18T= MANE Select	ENSP00000322450.6:n.1162+18T=
ENST00000647561.1:c.1162+18T=	ENSP00000497587.1:n.1162+18T=
ENST00000322776.10:c.1162+18T=	ENSP00000322450.6:n.1162+18T=
ENST00000415352.6:c.1141+18T=	ENSP00000395368.2:n.1141+18T=
ENST00000526770.5:n.1445+18T=
ENST00000527355.5:c.370-124T=	ENSP00000432637.1:n.370-124T=
ENST00000527923.1:n.504+18T=
ENST00000529927.5:c.1135+18T=	ENSP00000436766.1:n.1135+18T=
ENST00000531250.1:n.426+18T=
ENST00000532303.5:c.859+18T=	ENSP00000432015.1:n.859+18T=
ENST00000533919.5:c.566+18T=	ENSP00000435199.1:n.566+18T=
ENST00000534352.1:n.278T=
NM_001166102.1:c.1135+18T=	NP_001159574.1:n.1135+18T=
NM_007103.3:c.1162+18T=	NP_009034.2:n.1162+18T=
NM_001166102.2:c.1135+18T=	NP_001159574.1:n.1135+18T=
NM_007103.4:c.1162+18T= MANE Select	NP_009034.2:n.1162+18T=