Canonical Allele Identifier: CA381537595

Gene: NDUFV1

Linked Data

• MyVariant Identifiers: chr11:g.67378036A>G (hg19) ; chr11:g.67610565A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67610565A>G , CM000673.2:g.67610565A>G	GRCh38
NC_000011.9:g.67378036A>G , CM000673.1:g.67378036A>G	GRCh37
NC_000011.8:g.67134612A>G	NCBI36
NG_013353.1:g.8714A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322776.11:c.695A>G MANE Select	ENSP00000322450.6:p.Asp232Gly
ENST00000647561.1:c.695A>G	ENSP00000497587.1:p.Asp232Gly
ENST00000322776.10:c.695A>G	ENSP00000322450.6:p.Asp232Gly
ENST00000415352.6:c.674A>G	ENSP00000395368.2:p.Asp225Gly
ENST00000526169.1:n.437A>G
ENST00000526770.5:n.554A>G
ENST00000529927.5:c.668A>G	ENSP00000436766.1:p.Asp223Gly
ENST00000532244.5:c.392A>G	ENSP00000435202.1:p.Asp131Gly
ENST00000532303.5:c.392A>G	ENSP00000432015.1:p.Asp131Gly
ENST00000533919.5:c.173A>G	ENSP00000435199.1:p.Asp58Gly
NM_001166102.1:c.668A>G	NP_001159574.1:p.Asp223Gly
NM_007103.3:c.695A>G	NP_009034.2:p.Asp232Gly
NM_001166102.2:c.668A>G	NP_001159574.1:p.Asp223Gly
NM_007103.4:c.695A>G MANE Select	NP_009034.2:p.Asp232Gly