Canonical Allele Identifier: CA7932819

Gene: COQ7 COQ7-DT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.19067673C>T , CM000678.2:g.19067673C>T	GRCh38
NC_000016.9:g.19078995C>T , CM000678.1:g.19078995C>T	GRCh37
NC_000016.8:g.18986496C>T	NCBI36
NG_046596.1:g.5079C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321998.10:c.9C>T (COQ7) MANE Select	ENSP00000322316.5:p.Cys3=
ENST00000321998.9:c.9C>T (COQ7)	ENSP00000322316.5:p.Cys3=
ENST00000564746.1:n.28C>T (COQ7)
ENST00000566049.5:c.9C>T (COQ7)	ENSP00000456490.1:p.Cys3=
ENST00000566110.5:c.-250C>T (COQ7)	ENSP00000456943.1:n.-250C>T
ENST00000568985.5:c.9C>T (COQ7)	ENSP00000456734.1:p.Cys3=
ENST00000569312.5:c.9C>T (COQ7)	ENSP00000459076.1:p.Cys3=
NM_016138.4:c.9C>T (COQ7)	NP_057222.2:p.Cys3=
NR_119379.1:n.19G>A (COQ7-DT)
NR_119380.1:n.19G>A (COQ7-DT)
NR_119381.1:n.19G>A (COQ7-DT)
XR_950722.1:n.79C>T (COQ7)
XR_950722.3:n.79C>T (COQ7)
NM_016138.5:c.9C>T (COQ7) MANE Select	NP_057222.2:p.Cys3=
NM_001370490.1:c.9C>T (COQ7)	NP_001357419.1:p.Cys3=
NR_163448.1:n.60C>T (COQ7)
NR_163450.1:n.60C>T (COQ7)