Canonical Allele Identifier: CA475412375
Gene: NDUFV1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.67377911C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67610440C>T , CM000673.2:g.67610440C>T GRCh38
NC_000011.9:g.67377911C>T , CM000673.1:g.67377911C>T GRCh37
NC_000011.8:g.67134487C>T NCBI36
NG_013353.1:g.8589C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000322776.11:c.570C>T MANE Select ENSP00000322450.6:p.Gly190=
ENST00000647561.1:c.570C>T ENSP00000497587.1:p.Gly190=
ENST00000322776.10:c.570C>T ENSP00000322450.6:p.Gly190=
ENST00000415352.6:c.549C>T ENSP00000395368.2:p.Gly183=
ENST00000526169.1:n.312C>T
ENST00000526770.5:n.429C>T
ENST00000529867.5:c.534C>T ENSP00000434438.1:p.Gly178=
ENST00000529927.5:c.543C>T ENSP00000436766.1:p.Gly181=
ENST00000532244.5:c.267C>T ENSP00000435202.1:p.Gly89=
ENST00000532303.5:c.267C>T ENSP00000432015.1:p.Gly89=
ENST00000532343.5:c.267C>T ENSP00000431751.1:p.Gly89=
ENST00000533919.5:c.48C>T ENSP00000435199.1:p.Gly16=
NM_001166102.1:c.543C>T NP_001159574.1:p.Gly181=
NM_007103.3:c.570C>T NP_009034.2:p.Gly190=
NM_001166102.2:c.543C>T NP_001159574.1:p.Gly181=
NM_007103.4:c.570C>T MANE Select NP_009034.2:p.Gly190=