Canonical Allele Identifier: CA1980192063
Gene: NDUFV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67611520A= , CM000673.2:g.67611520A= GRCh38
NC_000011.9:g.67378991A= , CM000673.1:g.67378991A= GRCh37
NC_000011.8:g.67135567A= NCBI36
NG_013353.1:g.9669A=

Transcript Alleles

HGVS Amino-acid change
ENST00000322776.11:c.1031A= MANE Select ENSP00000322450.6:p.Gln344=
ENST00000647561.1:c.1031A= ENSP00000497587.1:p.Gln344=
ENST00000322776.10:c.1031A= ENSP00000322450.6:p.Gln344=
ENST00000415352.6:c.1010A= ENSP00000395368.2:p.Gln337=
ENST00000526169.1:n.656-2A=
ENST00000526770.5:n.1314A=
ENST00000527355.5:c.320A= ENSP00000432637.1:p.Gln107=
ENST00000527923.1:n.373A=
ENST00000529927.5:c.1004A= ENSP00000436766.1:p.Gln335=
ENST00000532303.5:c.728A= ENSP00000432015.1:p.Gln243=
ENST00000533919.5:c.435A= ENSP00000435199.1:n.435A=
NM_001166102.1:c.1004A= NP_001159574.1:p.Gln335=
NM_007103.3:c.1031A= NP_009034.2:p.Gln344=
NM_001166102.2:c.1004A= NP_001159574.1:p.Gln335=
NM_007103.4:c.1031A= MANE Select NP_009034.2:p.Gln344=