Canonical Allele Identifier: CA381537107

Gene: NDUFV1

Linked Data

• gnomAD v4: 11-67610510-G-C
• MyVariant Identifiers: chr11:g.67377981G>C (hg19) ; chr11:g.67610510G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67610510G>C , CM000673.2:g.67610510G>C	GRCh38
NC_000011.9:g.67377981G>C , CM000673.1:g.67377981G>C	GRCh37
NC_000011.8:g.67134557G>C	NCBI36
NG_013353.1:g.8659G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322776.11:c.640G>C MANE Select	ENSP00000322450.6:p.Glu214Gln
ENST00000647561.1:c.640G>C	ENSP00000497587.1:p.Glu214Gln
ENST00000322776.10:c.640G>C	ENSP00000322450.6:p.Glu214Gln
ENST00000415352.6:c.619G>C	ENSP00000395368.2:p.Glu207Gln
ENST00000526169.1:n.382G>C
ENST00000526770.5:n.499G>C
ENST00000529927.5:c.613G>C	ENSP00000436766.1:p.Glu205Gln
ENST00000532244.5:c.337G>C	ENSP00000435202.1:p.Glu113Gln
ENST00000532303.5:c.337G>C	ENSP00000432015.1:p.Glu113Gln
ENST00000533919.5:c.118G>C	ENSP00000435199.1:p.Glu40Gln
NM_001166102.1:c.613G>C	NP_001159574.1:p.Glu205Gln
NM_007103.3:c.640G>C	NP_009034.2:p.Glu214Gln
NM_001166102.2:c.613G>C	NP_001159574.1:p.Glu205Gln
NM_007103.4:c.640G>C MANE Select	NP_009034.2:p.Glu214Gln