Canonical Allele Identifier: CA381536522

Gene: NDUFV1

Linked Data

• MyVariant Identifiers: chr11:g.67377874A>T (hg19) ; chr11:g.67610403A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67610403A>T , CM000673.2:g.67610403A>T	GRCh38
NC_000011.9:g.67377874A>T , CM000673.1:g.67377874A>T	GRCh37
NC_000011.8:g.67134450A>T	NCBI36
NG_013353.1:g.8552A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322776.11:c.533A>T MANE Select	ENSP00000322450.6:p.Glu178Val
ENST00000647561.1:c.533A>T	ENSP00000497587.1:p.Glu178Val
ENST00000322776.10:c.533A>T	ENSP00000322450.6:p.Glu178Val
ENST00000415352.6:c.512A>T	ENSP00000395368.2:p.Glu171Val
ENST00000526169.1:n.275A>T
ENST00000526770.5:n.392A>T
ENST00000529867.5:c.497A>T	ENSP00000434438.1:p.Glu166Val
ENST00000529927.5:c.506A>T	ENSP00000436766.1:p.Glu169Val
ENST00000530638.1:c.416A>T	ENSP00000436936.1:p.Glu139Val
ENST00000532244.5:c.230A>T	ENSP00000435202.1:p.Glu77Val
ENST00000532303.5:c.230A>T	ENSP00000432015.1:p.Glu77Val
ENST00000532343.5:c.230A>T	ENSP00000431751.1:p.Glu77Val
ENST00000533075.5:c.512A>T	ENSP00000437267.1:p.Glu171Val
ENST00000533919.5:c.11A>T	ENSP00000435199.1:p.Glu4Val
NM_001166102.1:c.506A>T	NP_001159574.1:p.Glu169Val
NM_007103.3:c.533A>T	NP_009034.2:p.Glu178Val
NM_001166102.2:c.506A>T	NP_001159574.1:p.Glu169Val
NM_007103.4:c.533A>T MANE Select	NP_009034.2:p.Glu178Val