Canonical Allele Identifier: CA381537055

Gene: NDUFV1

Linked Data

• gnomAD v4: 11-67610499-C-G
• MyVariant Identifiers: chr11:g.67377970C>G (hg19) ; chr11:g.67610499C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67610499C>G , CM000673.2:g.67610499C>G	GRCh38
NC_000011.9:g.67377970C>G , CM000673.1:g.67377970C>G	GRCh37
NC_000011.8:g.67134546C>G	NCBI36
NG_013353.1:g.8648C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322776.11:c.629C>G MANE Select	ENSP00000322450.6:p.Thr210Arg
ENST00000647561.1:c.629C>G	ENSP00000497587.1:p.Thr210Arg
ENST00000322776.10:c.629C>G	ENSP00000322450.6:p.Thr210Arg
ENST00000415352.6:c.608C>G	ENSP00000395368.2:p.Thr203Arg
ENST00000526169.1:n.371C>G
ENST00000526770.5:n.488C>G
ENST00000529927.5:c.602C>G	ENSP00000436766.1:p.Thr201Arg
ENST00000532244.5:c.326C>G	ENSP00000435202.1:p.Thr109Arg
ENST00000532303.5:c.326C>G	ENSP00000432015.1:p.Thr109Arg
ENST00000533919.5:c.107C>G	ENSP00000435199.1:p.Thr36Arg
NM_001166102.1:c.602C>G	NP_001159574.1:p.Thr201Arg
NM_007103.3:c.629C>G	NP_009034.2:p.Thr210Arg
NM_001166102.2:c.602C>G	NP_001159574.1:p.Thr201Arg
NM_007103.4:c.629C>G MANE Select	NP_009034.2:p.Thr210Arg