Canonical Allele Identifier: CA381540458

Gene: NDUFV1

Linked Data

• MyVariant Identifiers: chr11:g.67378883C>G (hg19) ; chr11:g.67611412C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67611412C>G , CM000673.2:g.67611412C>G	GRCh38
NC_000011.9:g.67378883C>G , CM000673.1:g.67378883C>G	GRCh37
NC_000011.8:g.67135459C>G	NCBI36
NG_013353.1:g.9561C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000322776.11:c.923C>G MANE Select	ENSP00000322450.6:p.Thr308Arg
ENST00000647561.1:c.923C>G	ENSP00000497587.1:p.Thr308Arg
ENST00000322776.10:c.923C>G	ENSP00000322450.6:p.Thr308Arg
ENST00000415352.6:c.902C>G	ENSP00000395368.2:p.Thr301Arg
ENST00000526169.1:n.656-110C>G
ENST00000526770.5:n.1206C>G
ENST00000527355.5:c.212C>G	ENSP00000432637.1:p.Thr71Arg
ENST00000527923.1:n.265C>G
ENST00000529927.5:c.896C>G	ENSP00000436766.1:p.Thr299Arg
ENST00000532303.5:c.620C>G	ENSP00000432015.1:p.Thr207Arg
ENST00000533919.5:c.392-65C>G	ENSP00000435199.1:n.392-65C>G
NM_001166102.1:c.896C>G	NP_001159574.1:p.Thr299Arg
NM_007103.3:c.923C>G	NP_009034.2:p.Thr308Arg
NM_001166102.2:c.896C>G	NP_001159574.1:p.Thr299Arg
NM_007103.4:c.923C>G MANE Select	NP_009034.2:p.Thr308Arg