Canonical Allele Identifier: CA1980191735

Gene: NDUFV1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67611427_67611430delinsACCT , CM000673.2:g.67611427_67611430delinsACCT	GRCh38
NC_000011.9:g.67378898_67378901delinsACCT , CM000673.1:g.67378898_67378901delinsACCT	GRCh37
NC_000011.8:g.67135474_67135477delinsACCT	NCBI36
NG_013353.1:g.9576_9579delinsACCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322776.11:c.938_941delinsACCT MANE Select	ENSP00000322450.6:p.Asn313=
ENST00000647561.1:c.938_941delinsACCT	ENSP00000497587.1:p.Asn313=
ENST00000322776.10:c.938_941delinsACCT	ENSP00000322450.6:p.Asn313=
ENST00000415352.6:c.917_920delinsACCT	ENSP00000395368.2:p.Asn306=
ENST00000526169.1:n.656-95_656-92delinsACCT
ENST00000526770.5:n.1221_1224delinsACCT
ENST00000527355.5:c.227_230delinsACCT	ENSP00000432637.1:p.Asn76=
ENST00000527923.1:n.280_283delinsACCT
ENST00000529927.5:c.911_914delinsACCT	ENSP00000436766.1:p.Asn304=
ENST00000532303.5:c.635_638delinsACCT	ENSP00000432015.1:p.Asn212=
ENST00000533919.5:c.392-50_392-47delinsACCT	ENSP00000435199.1:n.392-50_392-47delinsACCT
NM_001166102.1:c.911_914delinsACCT	NP_001159574.1:p.Asn304=
NM_007103.3:c.938_941delinsACCT	NP_009034.2:p.Asn313=
NM_001166102.2:c.911_914delinsACCT	NP_001159574.1:p.Asn304=
NM_007103.4:c.938_941delinsACCT MANE Select	NP_009034.2:p.Asn313=