Canonical Allele Identifier: CA475412280
Gene: NDUFV1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.67377893G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67610422G>A , CM000673.2:g.67610422G>A GRCh38
NC_000011.9:g.67377893G>A , CM000673.1:g.67377893G>A GRCh37
NC_000011.8:g.67134469G>A NCBI36
NG_013353.1:g.8571G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000322776.11:c.552G>A MANE Select ENSP00000322450.6:p.Lys184=
ENST00000647561.1:c.552G>A ENSP00000497587.1:p.Lys184=
ENST00000322776.10:c.552G>A ENSP00000322450.6:p.Lys184=
ENST00000415352.6:c.531G>A ENSP00000395368.2:p.Lys177=
ENST00000526169.1:n.294G>A
ENST00000526770.5:n.411G>A
ENST00000529867.5:c.516G>A ENSP00000434438.1:p.Lys172=
ENST00000529927.5:c.525G>A ENSP00000436766.1:p.Lys175=
ENST00000532244.5:c.249G>A ENSP00000435202.1:p.Lys83=
ENST00000532303.5:c.249G>A ENSP00000432015.1:p.Lys83=
ENST00000532343.5:c.249G>A ENSP00000431751.1:p.Lys83=
ENST00000533075.5:c.531G>A ENSP00000437267.1:p.Lys177=
ENST00000533919.5:c.30G>A ENSP00000435199.1:p.Lys10=
NM_001166102.1:c.525G>A NP_001159574.1:p.Lys175=
NM_007103.3:c.552G>A NP_009034.2:p.Lys184=
NM_001166102.2:c.525G>A NP_001159574.1:p.Lys175=
NM_007103.4:c.552G>A MANE Select NP_009034.2:p.Lys184=