Canonical Allele Identifier: CA1980188127

Gene: NDUFV1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67609382_67609383delinsTG , CM000673.2:g.67609382_67609383delinsTG	GRCh38
NC_000011.9:g.67376853_67376854delinsTG , CM000673.1:g.67376853_67376854delinsTG	GRCh37
NC_000011.8:g.67133429_67133430delinsTG	NCBI36
NG_013353.1:g.7531_7532delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322776.11:c.327-70_327-69delinsTG MANE Select	ENSP00000322450.6:n.327-70_327-69delinsTG
ENST00000647561.1:c.327-70_327-69delinsTG	ENSP00000497587.1:n.327-70_327-69delinsTG
ENST00000322776.10:c.327-70_327-69delinsTG	ENSP00000322450.6:n.327-70_327-69delinsTG
ENST00000415352.6:c.306-70_306-69delinsTG	ENSP00000395368.2:n.306-70_306-69delinsTG
ENST00000524838.5:n.384-70_384-69delinsTG
ENST00000525086.5:n.374-44_374-43delinsTG
ENST00000526169.1:n.69-70_69-69delinsTG
ENST00000526770.5:n.186-70_186-69delinsTG
ENST00000528314.1:c.24-70_24-69delinsTG	ENSP00000434581.1:n.24-70_24-69delinsTG
ENST00000528377.1:n.498-70_498-69delinsTG
ENST00000529867.5:c.291-70_291-69delinsTG	ENSP00000434438.1:n.291-70_291-69delinsTG
ENST00000529927.5:c.300-70_300-69delinsTG	ENSP00000436766.1:n.300-70_300-69delinsTG
ENST00000530014.5:n.622-70_622-69delinsTG
ENST00000530103.5:c.*221-70_*221-69delinsTG	ENSP00000434575.1:n.*221-70_*221-69delinsTG
ENST00000530638.1:c.210-70_210-69delinsTG	ENSP00000436936.1:n.210-70_210-69delinsTG
ENST00000532244.5:c.24-70_24-69delinsTG	ENSP00000435202.1:n.24-70_24-69delinsTG
ENST00000532303.5:c.24-70_24-69delinsTG	ENSP00000432015.1:n.24-70_24-69delinsTG
ENST00000532343.5:c.24-70_24-69delinsTG	ENSP00000431751.1:n.24-70_24-69delinsTG
ENST00000533075.5:c.306-70_306-69delinsTG	ENSP00000437267.1:n.306-70_306-69delinsTG
ENST00000534139.5:n.443-70_443-69delinsTG
NM_001166102.1:c.300-70_300-69delinsTG	NP_001159574.1:n.300-70_300-69delinsTG
NM_007103.3:c.327-70_327-69delinsTG	NP_009034.2:n.327-70_327-69delinsTG
NM_001166102.2:c.300-70_300-69delinsTG	NP_001159574.1:n.300-70_300-69delinsTG
NM_007103.4:c.327-70_327-69delinsTG MANE Select	NP_009034.2:n.327-70_327-69delinsTG