Canonical Allele Identifier: CA475412340

Gene: NDUFV1

Linked Data

• MyVariant Identifiers: chr11:g.67377905C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67610434C>A , CM000673.2:g.67610434C>A	GRCh38
NC_000011.9:g.67377905C>A , CM000673.1:g.67377905C>A	GRCh37
NC_000011.8:g.67134481C>A	NCBI36
NG_013353.1:g.8583C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322776.11:c.564C>A MANE Select	ENSP00000322450.6:p.Gly188=
ENST00000647561.1:c.564C>A	ENSP00000497587.1:p.Gly188=
ENST00000322776.10:c.564C>A	ENSP00000322450.6:p.Gly188=
ENST00000415352.6:c.543C>A	ENSP00000395368.2:p.Gly181=
ENST00000526169.1:n.306C>A
ENST00000526770.5:n.423C>A
ENST00000529867.5:c.528C>A	ENSP00000434438.1:p.Gly176=
ENST00000529927.5:c.537C>A	ENSP00000436766.1:p.Gly179=
ENST00000532244.5:c.261C>A	ENSP00000435202.1:p.Gly87=
ENST00000532303.5:c.261C>A	ENSP00000432015.1:p.Gly87=
ENST00000532343.5:c.261C>A	ENSP00000431751.1:p.Gly87=
ENST00000533919.5:c.42C>A	ENSP00000435199.1:p.Gly14=
NM_001166102.1:c.537C>A	NP_001159574.1:p.Gly179=
NM_007103.3:c.564C>A	NP_009034.2:p.Gly188=
NM_001166102.2:c.537C>A	NP_001159574.1:p.Gly179=
NM_007103.4:c.564C>A MANE Select	NP_009034.2:p.Gly188=