Canonical Allele Identifier: CA381537584

Gene: NDUFV1

Linked Data

• MyVariant Identifiers: chr11:g.67378035G>A (hg19) ; chr11:g.67610564G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67610564G>A , CM000673.2:g.67610564G>A	GRCh38
NC_000011.9:g.67378035G>A , CM000673.1:g.67378035G>A	GRCh37
NC_000011.8:g.67134611G>A	NCBI36
NG_013353.1:g.8713G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322776.11:c.694G>A MANE Select	ENSP00000322450.6:p.Asp232Asn
ENST00000647561.1:c.694G>A	ENSP00000497587.1:p.Asp232Asn
ENST00000322776.10:c.694G>A	ENSP00000322450.6:p.Asp232Asn
ENST00000415352.6:c.673G>A	ENSP00000395368.2:p.Asp225Asn
ENST00000526169.1:n.436G>A
ENST00000526770.5:n.553G>A
ENST00000529927.5:c.667G>A	ENSP00000436766.1:p.Asp223Asn
ENST00000532244.5:c.391G>A	ENSP00000435202.1:p.Asp131Asn
ENST00000532303.5:c.391G>A	ENSP00000432015.1:p.Asp131Asn
ENST00000533919.5:c.172G>A	ENSP00000435199.1:p.Asp58Asn
NM_001166102.1:c.667G>A	NP_001159574.1:p.Asp223Asn
NM_007103.3:c.694G>A	NP_009034.2:p.Asp232Asn
NM_001166102.2:c.667G>A	NP_001159574.1:p.Asp223Asn
NM_007103.4:c.694G>A MANE Select	NP_009034.2:p.Asp232Asn