Canonical Allele Identifier: CA493822194

Gene: COQ7

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.19072073C>G , CM000678.2:g.19072073C>G	GRCh38
NC_000016.9:g.19083395C>G , CM000678.1:g.19083395C>G	GRCh37
NC_000016.8:g.18990896C>G	NCBI36
NG_046596.1:g.9479C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321998.10:c.219C>G MANE Select	ENSP00000322316.5:p.Val73=
ENST00000321998.9:c.219C>G	ENSP00000322316.5:p.Val73=
ENST00000544894.6:c.105C>G	ENSP00000442923.2:p.Val35=
ENST00000561858.5:c.105C>G	ENSP00000457256.1:p.Val35=
ENST00000564746.1:n.238C>G
ENST00000566049.5:c.219C>G	ENSP00000456490.1:p.Val73=
ENST00000566110.5:c.105C>G	ENSP00000456943.1:p.Val35=
ENST00000568985.5:c.219C>G	ENSP00000456734.1:p.Val73=
ENST00000569127.1:c.150C>G	ENSP00000455122.1:p.Val50=
ENST00000569312.5:c.219C>G	ENSP00000459076.1:p.Val73=
NM_001190983.1:c.105C>G	NP_001177912.1:p.Val35=
NM_016138.4:c.219C>G	NP_057222.2:p.Val73=
XR_950722.1:n.289C>G
XM_024450140.1:c.177C>G	XP_024305908.1:p.Val59=
XM_024450141.1:c.105C>G	XP_024305909.1:p.Val35=
XR_950722.3:n.289C>G
NM_016138.5:c.219C>G MANE Select	NP_057222.2:p.Val73=
NM_001190983.2:c.105C>G	NP_001177912.1:p.Val35=
NM_001370489.1:c.177C>G	NP_001357418.1:p.Val59=
NM_001370490.1:c.219C>G	NP_001357419.1:p.Val73=
NM_001370491.1:c.177C>G	NP_001357420.1:p.Val59=
NM_001370492.1:c.105C>G	NP_001357421.1:p.Val35=
NM_001370493.1:c.105C>G	NP_001357422.1:p.Val35=
NM_001370494.1:c.105C>G	NP_001357423.1:p.Val35=
NM_001370495.1:c.105C>G	NP_001357424.1:p.Val35=
NR_163448.1:n.270C>G
NR_163449.1:n.248C>G
NR_163450.1:n.270C>G