Canonical Allele Identifier: CA1980191693

Gene: NDUFV1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67611411_67611412delinsAC , CM000673.2:g.67611411_67611412delinsAC	GRCh38
NC_000011.9:g.67378882_67378883delinsAC , CM000673.1:g.67378882_67378883delinsAC	GRCh37
NC_000011.8:g.67135458_67135459delinsAC	NCBI36
NG_013353.1:g.9560_9561delinsAC

Transcript Alleles

HGVS	Amino-acid change
ENST00000322776.11:c.922_923delinsAC MANE Select	ENSP00000322450.6:p.Thr308=
ENST00000647561.1:c.922_923delinsAC	ENSP00000497587.1:p.Thr308=
ENST00000322776.10:c.922_923delinsAC	ENSP00000322450.6:p.Thr308=
ENST00000415352.6:c.901_902delinsAC	ENSP00000395368.2:p.Thr301=
ENST00000526169.1:n.656-111_656-110delinsAC
ENST00000526770.5:n.1205_1206delinsAC
ENST00000527355.5:c.211_212delinsAC	ENSP00000432637.1:p.Thr71=
ENST00000527923.1:n.264_265delinsAC
ENST00000529927.5:c.895_896delinsAC	ENSP00000436766.1:p.Thr299=
ENST00000532303.5:c.619_620delinsAC	ENSP00000432015.1:p.Thr207=
ENST00000533919.5:c.392-66_392-65delinsAC	ENSP00000435199.1:n.392-66_392-65delinsAC...
NM_001166102.1:c.895_896delinsAC	NP_001159574.1:p.Thr299=
NM_007103.3:c.922_923delinsAC	NP_009034.2:p.Thr308=
NM_001166102.2:c.895_896delinsAC	NP_001159574.1:p.Thr299=
NM_007103.4:c.922_923delinsAC MANE Select	NP_009034.2:p.Thr308=