Canonical Allele Identifier: CA381537567

Gene: NDUFV1

Linked Data

• MyVariant Identifiers: chr11:g.67378033C>T (hg19) ; chr11:g.67610562C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67610562C>T , CM000673.2:g.67610562C>T	GRCh38
NC_000011.9:g.67378033C>T , CM000673.1:g.67378033C>T	GRCh37
NC_000011.8:g.67134609C>T	NCBI36
NG_013353.1:g.8711C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322776.11:c.692C>T MANE Select	ENSP00000322450.6:p.Ala231Val
ENST00000647561.1:c.692C>T	ENSP00000497587.1:p.Ala231Val
ENST00000322776.10:c.692C>T	ENSP00000322450.6:p.Ala231Val
ENST00000415352.6:c.671C>T	ENSP00000395368.2:p.Ala224Val
ENST00000526169.1:n.434C>T
ENST00000526770.5:n.551C>T
ENST00000529927.5:c.665C>T	ENSP00000436766.1:p.Ala222Val
ENST00000532244.5:c.389C>T	ENSP00000435202.1:p.Ala130Val
ENST00000532303.5:c.389C>T	ENSP00000432015.1:p.Ala130Val
ENST00000533919.5:c.170C>T	ENSP00000435199.1:p.Ala57Val
NM_001166102.1:c.665C>T	NP_001159574.1:p.Ala222Val
NM_007103.3:c.692C>T	NP_009034.2:p.Ala231Val
NM_001166102.2:c.665C>T	NP_001159574.1:p.Ala222Val
NM_007103.4:c.692C>T MANE Select	NP_009034.2:p.Ala231Val