Canonical Allele Identifier: CA390374855

Gene: COQ6 ENTPD5

Linked Data

• MyVariant Identifiers: chr14:g.74424859C>G (hg19) ; chr14:g.73958156C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.73958156C>G , CM000676.2:g.73958156C>G	GRCh38
NC_000014.8:g.74424859C>G , CM000676.1:g.74424859C>G	GRCh37
NC_000014.7:g.73494612C>G	NCBI36
NG_032805.1:g.13223C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000334571.7:c.491C>G (COQ6) MANE Select	ENSP00000333946.2:p.Thr164Arg
ENST00000238709.8:c.488C>G (COQ6)	ENSP00000238709.5:p.Thr163Arg
ENST00000334571.6:c.491C>G (COQ6)	ENSP00000333946.2:p.Thr164Arg
ENST00000394026.8:c.416C>G (COQ6)	ENSP00000377594.4:p.Thr139Arg
ENST00000553462.6:n.339C>G (COQ6)
ENST00000554153.5:c.*96C>G (COQ6)	ENSP00000451685.1:n.*96C>G
ENST00000554320.1:c.266C>G (COQ6)	ENSP00000451123.1:p.Thr89Arg
ENST00000554341.6:c.*96C>G (COQ6)	ENSP00000450736.2:n.*96C>G
ENST00000554920.5:c.481+2228C>G (COQ6)	ENSP00000451562.1:n.481+2228C>G
ENST00000555511.5:n.609C>G (COQ6)
ENST00000556300.6:n.525C>G (COQ6)
ENST00000557205.6:n.455C>G (COQ6)
ENST00000557325.5:c.*1374G>C (ENTPD5)	ENSP00000451810.1:n.*1374G>C
ENST00000557584.5:c.*96C>G (COQ6)	ENSP00000450511.1:n.*96C>G
ENST00000629426.2:c.266C>G (COQ6)	ENSP00000486650.1:p.Thr89Arg
NM_182476.2:c.491C>G (COQ6)	NP_872282.1:p.Thr164Arg
NM_182480.2:c.416C>G (COQ6)	NP_872286.2:p.Thr139Arg
XM_005267716.1:c.326C>G (COQ6)	XP_005267773.1:p.Thr109Arg
XM_006720156.1:c.164C>G (COQ6)	XP_006720219.1:p.Thr55Arg
XM_011536807.1:c.491C>G (COQ6)	XP_011535109.1:p.Thr164Arg
XM_011536808.1:c.266C>G (COQ6)	XP_011535110.1:p.Thr89Arg
XM_011536809.1:c.266C>G (COQ6)	XP_011535111.1:p.Thr89Arg
XM_011536810.1:c.491C>G (COQ6)	XP_011535112.1:p.Thr164Arg
XM_011536811.1:c.73-815C>G (COQ6)	XP_011535113.1:n.73-815C>G
XR_943465.1:n.544C>G (COQ6)
XR_943466.1:n.544C>G (COQ6)
NM_001330189.1:c.*1374G>C (ENTPD5)	NP_001317118.1:n.*1374G>C
XM_011536807.2:c.491C>G (COQ6)	XP_011535109.1:p.Thr164Arg
XM_011536808.2:c.266C>G (COQ6)	XP_011535110.1:p.Thr89Arg
XM_011536809.3:c.266C>G (COQ6)	XP_011535111.1:p.Thr89Arg
XM_011536810.3:c.491C>G (COQ6)	XP_011535112.1:p.Thr164Arg
XM_017021351.2:c.73-815C>G (COQ6)	XP_016876840.1:n.73-815C>G
XM_017021352.2:c.-809C>G (COQ6)	XP_016876841.1:n.-809C>G
XM_024449619.1:c.-258C>G (COQ6)	XP_024305387.1:n.-258C>G
XR_001750342.1:n.455C>G (COQ6)
XR_943465.3:n.521C>G (COQ6)
XR_943466.3:n.521C>G (COQ6)
NM_001330189.2:c.*1374G>C (ENTPD5)	NP_001317118.1:n.*1374G>C
NM_182476.3:c.491C>G (COQ6) MANE Select	NP_872282.1:p.Thr164Arg
NM_001382258.1:c.1201-2569G>C (ENTPD5)	NP_001369187.1:n.1201-2569G>C
NM_001382259.1:c.*1374G>C (ENTPD5)	NP_001369188.1:n.*1374G>C
NM_001382260.1:c.*1374G>C (ENTPD5)	NP_001369189.1:n.*1374G>C
NM_001382262.1:c.1201-2328G>C (ENTPD5)	NP_001369191.1:n.1201-2328G>C
NM_182480.3:c.416C>G (COQ6)	NP_872286.2:p.Thr139Arg