Canonical Allele Identifier: CA381536681

Gene: NDUFV1

Linked Data

• MyVariant Identifiers: chr11:g.67377900T>G (hg19) ; chr11:g.67610429T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67610429T>G , CM000673.2:g.67610429T>G	GRCh38
NC_000011.9:g.67377900T>G , CM000673.1:g.67377900T>G	GRCh37
NC_000011.8:g.67134476T>G	NCBI36
NG_013353.1:g.8578T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322776.11:c.559T>G MANE Select	ENSP00000322450.6:p.Cys187Gly
ENST00000647561.1:c.559T>G	ENSP00000497587.1:p.Cys187Gly
ENST00000322776.10:c.559T>G	ENSP00000322450.6:p.Cys187Gly
ENST00000415352.6:c.538T>G	ENSP00000395368.2:p.Cys180Gly
ENST00000526169.1:n.301T>G
ENST00000526770.5:n.418T>G
ENST00000529867.5:c.523T>G	ENSP00000434438.1:p.Cys175Gly
ENST00000529927.5:c.532T>G	ENSP00000436766.1:p.Cys178Gly
ENST00000532244.5:c.256T>G	ENSP00000435202.1:p.Cys86Gly
ENST00000532303.5:c.256T>G	ENSP00000432015.1:p.Cys86Gly
ENST00000532343.5:c.256T>G	ENSP00000431751.1:p.Cys86Gly
ENST00000533919.5:c.37T>G	ENSP00000435199.1:p.Cys13Gly
NM_001166102.1:c.532T>G	NP_001159574.1:p.Cys178Gly
NM_007103.3:c.559T>G	NP_009034.2:p.Cys187Gly
NM_001166102.2:c.532T>G	NP_001159574.1:p.Cys178Gly
NM_007103.4:c.559T>G MANE Select	NP_009034.2:p.Cys187Gly