Canonical Allele Identifier: CA1980192049
Gene: NDUFV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67611516G= , CM000673.2:g.67611516G= GRCh38
NC_000011.9:g.67378987G= , CM000673.1:g.67378987G= GRCh37
NC_000011.8:g.67135563G= NCBI36
NG_013353.1:g.9665G=

Transcript Alleles

HGVS Amino-acid change
ENST00000322776.11:c.1027G= MANE Select ENSP00000322450.6:p.Val343=
ENST00000647561.1:c.1027G= ENSP00000497587.1:p.Val343=
ENST00000322776.10:c.1027G= ENSP00000322450.6:p.Val343=
ENST00000415352.6:c.1006G= ENSP00000395368.2:p.Val336=
ENST00000526169.1:n.656-6G=
ENST00000526770.5:n.1310G=
ENST00000527355.5:c.316G= ENSP00000432637.1:p.Val106=
ENST00000527923.1:n.369G=
ENST00000529927.5:c.1000G= ENSP00000436766.1:p.Val334=
ENST00000532303.5:c.724G= ENSP00000432015.1:p.Val242=
ENST00000533919.5:c.431G= ENSP00000435199.1:n.431G=
NM_001166102.1:c.1000G= NP_001159574.1:p.Val334=
NM_007103.3:c.1027G= NP_009034.2:p.Val343=
NM_001166102.2:c.1000G= NP_001159574.1:p.Val334=
NM_007103.4:c.1027G= MANE Select NP_009034.2:p.Val343=