Canonical Allele Identifier: CA475412210
Gene: NDUFV1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.67377881T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67610410T>C , CM000673.2:g.67610410T>C GRCh38
NC_000011.9:g.67377881T>C , CM000673.1:g.67377881T>C GRCh37
NC_000011.8:g.67134457T>C NCBI36
NG_013353.1:g.8559T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000322776.11:c.540T>C MANE Select ENSP00000322450.6:p.Gly180=
ENST00000647561.1:c.540T>C ENSP00000497587.1:p.Gly180=
ENST00000322776.10:c.540T>C ENSP00000322450.6:p.Gly180=
ENST00000415352.6:c.519T>C ENSP00000395368.2:p.Gly173=
ENST00000526169.1:n.282T>C
ENST00000526770.5:n.399T>C
ENST00000529867.5:c.504T>C ENSP00000434438.1:p.Gly168=
ENST00000529927.5:c.513T>C ENSP00000436766.1:p.Gly171=
ENST00000530638.1:c.423T>C ENSP00000436936.1:p.Gly141=
ENST00000532244.5:c.237T>C ENSP00000435202.1:p.Gly79=
ENST00000532303.5:c.237T>C ENSP00000432015.1:p.Gly79=
ENST00000532343.5:c.237T>C ENSP00000431751.1:p.Gly79=
ENST00000533075.5:c.519T>C ENSP00000437267.1:p.Gly173=
ENST00000533919.5:c.18T>C ENSP00000435199.1:p.Gly6=
NM_001166102.1:c.513T>C NP_001159574.1:p.Gly171=
NM_007103.3:c.540T>C NP_009034.2:p.Gly180=
NM_001166102.2:c.513T>C NP_001159574.1:p.Gly171=
NM_007103.4:c.540T>C MANE Select NP_009034.2:p.Gly180=