Canonical Allele Identifier: CA381540727

Gene: NDUFV1

Linked Data

• dbSNP Id: rs1481421987
• MyVariant Identifiers: chr11:g.67378933C>A (hg19) ; chr11:g.67611462C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67611462C>A , CM000673.2:g.67611462C>A	GRCh38
NC_000011.9:g.67378933C>A , CM000673.1:g.67378933C>A	GRCh37
NC_000011.8:g.67135509C>A	NCBI36
NG_013353.1:g.9611C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322776.11:c.973C>A MANE Select	ENSP00000322450.6:p.Pro325Thr
ENST00000647561.1:c.973C>A	ENSP00000497587.1:p.Pro325Thr
ENST00000322776.10:c.973C>A	ENSP00000322450.6:p.Pro325Thr
ENST00000415352.6:c.952C>A	ENSP00000395368.2:p.Pro318Thr
ENST00000526169.1:n.656-60C>A
ENST00000526770.5:n.1256C>A
ENST00000527355.5:c.262C>A	ENSP00000432637.1:p.Pro88Thr
ENST00000527923.1:n.315C>A
ENST00000529927.5:c.946C>A	ENSP00000436766.1:p.Pro316Thr
ENST00000532303.5:c.670C>A	ENSP00000432015.1:p.Pro224Thr
ENST00000533919.5:c.392-15C>A	ENSP00000435199.1:n.392-15C>A
NM_001166102.1:c.946C>A	NP_001159574.1:p.Pro316Thr
NM_007103.3:c.973C>A	NP_009034.2:p.Pro325Thr
NM_001166102.2:c.946C>A	NP_001159574.1:p.Pro316Thr
NM_007103.4:c.973C>A MANE Select	NP_009034.2:p.Pro325Thr