Canonical Allele Identifier: CA381537712

Gene: NDUFV1

Linked Data

• MyVariant Identifiers: chr11:g.67378050T>G (hg19) ; chr11:g.67610579T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67610579T>G , CM000673.2:g.67610579T>G	GRCh38
NC_000011.9:g.67378050T>G , CM000673.1:g.67378050T>G	GRCh37
NC_000011.8:g.67134626T>G	NCBI36
NG_013353.1:g.8728T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322776.11:c.700+9T>G MANE Select	ENSP00000322450.6:n.700+9T>G
ENST00000647561.1:c.700+9T>G	ENSP00000497587.1:n.700+9T>G
ENST00000322776.10:c.700+9T>G	ENSP00000322450.6:n.700+9T>G
ENST00000415352.6:c.679+9T>G	ENSP00000395368.2:n.679+9T>G
ENST00000526169.1:n.442+9T>G
ENST00000526770.5:n.568T>G
ENST00000529927.5:c.673+9T>G	ENSP00000436766.1:n.673+9T>G
ENST00000532244.5:c.406T>G	ENSP00000435202.1:p.Trp136Gly
ENST00000532303.5:c.397+9T>G	ENSP00000432015.1:n.397+9T>G
ENST00000533919.5:c.178+9T>G	ENSP00000435199.1:n.178+9T>G
NM_001166102.1:c.673+9T>G	NP_001159574.1:n.673+9T>G
NM_007103.3:c.700+9T>G	NP_009034.2:n.700+9T>G
NM_001166102.2:c.673+9T>G	NP_001159574.1:n.673+9T>G
NM_007103.4:c.700+9T>G MANE Select	NP_009034.2:n.700+9T>G