Canonical Allele Identifier: CA381540656

Gene: NDUFV1

Linked Data

• MyVariant Identifiers: chr11:g.67378922G>T (hg19) ; chr11:g.67611451G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67611451G>T , CM000673.2:g.67611451G>T	GRCh38
NC_000011.9:g.67378922G>T , CM000673.1:g.67378922G>T	GRCh37
NC_000011.8:g.67135498G>T	NCBI36
NG_013353.1:g.9600G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322776.11:c.962G>T MANE Select	ENSP00000322450.6:p.Gly321Val
ENST00000647561.1:c.962G>T	ENSP00000497587.1:p.Gly321Val
ENST00000322776.10:c.962G>T	ENSP00000322450.6:p.Gly321Val
ENST00000415352.6:c.941G>T	ENSP00000395368.2:p.Gly314Val
ENST00000526169.1:n.656-71G>T
ENST00000526770.5:n.1245G>T
ENST00000527355.5:c.251G>T	ENSP00000432637.1:p.Gly84Val
ENST00000527923.1:n.304G>T
ENST00000529927.5:c.935G>T	ENSP00000436766.1:p.Gly312Val
ENST00000532303.5:c.659G>T	ENSP00000432015.1:p.Gly220Val
ENST00000533919.5:c.392-26G>T	ENSP00000435199.1:n.392-26G>T
NM_001166102.1:c.935G>T	NP_001159574.1:p.Gly312Val
NM_007103.3:c.962G>T	NP_009034.2:p.Gly321Val
NM_001166102.2:c.935G>T	NP_001159574.1:p.Gly312Val
NM_007103.4:c.962G>T MANE Select	NP_009034.2:p.Gly321Val