Canonical Allele Identifier: CA475412893
Gene: NDUFV1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.67378025C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67610554C>G , CM000673.2:g.67610554C>G GRCh38
NC_000011.9:g.67378025C>G , CM000673.1:g.67378025C>G GRCh37
NC_000011.8:g.67134601C>G NCBI36
NG_013353.1:g.8703C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000322776.11:c.684C>G MANE Select ENSP00000322450.6:p.Pro228=
ENST00000647561.1:c.684C>G ENSP00000497587.1:p.Pro228=
ENST00000322776.10:c.684C>G ENSP00000322450.6:p.Pro228=
ENST00000415352.6:c.663C>G ENSP00000395368.2:p.Pro221=
ENST00000526169.1:n.426C>G
ENST00000526770.5:n.543C>G
ENST00000529927.5:c.657C>G ENSP00000436766.1:p.Pro219=
ENST00000532244.5:c.381C>G ENSP00000435202.1:p.Pro127=
ENST00000532303.5:c.381C>G ENSP00000432015.1:p.Pro127=
ENST00000533919.5:c.162C>G ENSP00000435199.1:p.Pro54=
NM_001166102.1:c.657C>G NP_001159574.1:p.Pro219=
NM_007103.3:c.684C>G NP_009034.2:p.Pro228=
NM_001166102.2:c.657C>G NP_001159574.1:p.Pro219=
NM_007103.4:c.684C>G MANE Select NP_009034.2:p.Pro228=