Canonical Allele Identifier: CA381540973
Gene: NDUFV1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67611522G>C , CM000673.2:g.67611522G>C GRCh38
NC_000011.9:g.67378993G>C , CM000673.1:g.67378993G>C GRCh37
NC_000011.8:g.67135569G>C NCBI36
NG_013353.1:g.9671G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000322776.11:c.1033G>C MANE Select ENSP00000322450.6:p.Ala345Pro
ENST00000647561.1:c.1033G>C ENSP00000497587.1:p.Ala345Pro
ENST00000322776.10:c.1033G>C ENSP00000322450.6:p.Ala345Pro
ENST00000415352.6:c.1012G>C ENSP00000395368.2:p.Ala338Pro
ENST00000526169.1:n.656G>C
ENST00000526770.5:n.1316G>C
ENST00000527355.5:c.322G>C ENSP00000432637.1:p.Ala108Pro
ENST00000527923.1:n.375G>C
ENST00000529927.5:c.1006G>C ENSP00000436766.1:p.Ala336Pro
ENST00000532303.5:c.730G>C ENSP00000432015.1:p.Ala244Pro
ENST00000533919.5:c.437G>C ENSP00000435199.1:n.437G>C
NM_001166102.1:c.1006G>C NP_001159574.1:p.Ala336Pro
NM_007103.3:c.1033G>C NP_009034.2:p.Ala345Pro
NM_001166102.2:c.1006G>C NP_001159574.1:p.Ala336Pro
NM_007103.4:c.1033G>C MANE Select NP_009034.2:p.Ala345Pro