Canonical Allele Identifier: CA394916981
Gene: COQ7 HGNC NCBI
COQ7-DT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.19067684C>G , CM000678.2:g.19067684C>G GRCh38
NC_000016.9:g.19079006C>G , CM000678.1:g.19079006C>G GRCh37
NC_000016.8:g.18986507C>G NCBI36
NG_046596.1:g.5090C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000321998.10:c.20C>G (COQ7) MANE Select ENSP00000322316.5:p.Ala7Gly
ENST00000321998.9:c.20C>G (COQ7) ENSP00000322316.5:p.Ala7Gly
ENST00000564746.1:n.39C>G (COQ7)
ENST00000566049.5:c.20C>G (COQ7) ENSP00000456490.1:p.Ala7Gly
ENST00000566110.5:c.-239C>G (COQ7) ENSP00000456943.1:n.-239C>G
ENST00000568985.5:c.20C>G (COQ7) ENSP00000456734.1:p.Ala7Gly
ENST00000569312.5:c.20C>G (COQ7) ENSP00000459076.1:p.Ala7Gly
NM_016138.4:c.20C>G (COQ7) NP_057222.2:p.Ala7Gly
NR_119379.1:n.8G>C (COQ7-DT)
NR_119380.1:n.8G>C (COQ7-DT)
NR_119381.1:n.8G>C (COQ7-DT)
XR_950722.1:n.90C>G (COQ7)
XR_950722.3:n.90C>G (COQ7)
NM_016138.5:c.20C>G (COQ7) MANE Select NP_057222.2:p.Ala7Gly
NM_001370490.1:c.20C>G (COQ7) NP_001357419.1:p.Ala7Gly
NR_163448.1:n.71C>G (COQ7)
NR_163450.1:n.71C>G (COQ7)