Canonical Allele Identifier: CA7264536

Gene: COQ6 ENTPD5

Linked Data

• dbSNP Id: rs755660869
• ExAC: 14:74429686 C / T
• gnomAD v2: 14-74429686-C-T
• gnomAD v4: 14-73962983-C-T
• MyVariant Identifiers: chr14:g.74429686C>T (hg19) ; chr14:g.73962983C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.73962983C>T , CM000676.2:g.73962983C>T	GRCh38
NC_000014.8:g.74429686C>T , CM000676.1:g.74429686C>T	GRCh37
NC_000014.7:g.73499439C>T	NCBI36
NG_032805.1:g.18050C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000334571.7:c.1391C>T (COQ6) MANE Select	ENSP00000333946.2:p.Ala464Val
ENST00000238709.8:c.1388C>T (COQ6)	ENSP00000238709.5:p.Ala463Val
ENST00000334571.6:c.1391C>T (COQ6)	ENSP00000333946.2:p.Ala464Val
ENST00000334696.10:c.*3945G>A (ENTPD5)	ENSP00000335246.6:n.*3945G>A
ENST00000394026.8:c.1316C>T (COQ6)	ENSP00000377594.4:p.Ala439Val
ENST00000554341.6:c.*990C>T (COQ6)	ENSP00000450736.2:n.*990C>T
ENST00000554920.5:c.495C>T (COQ6)	ENSP00000451562.1:p.Gly165=
ENST00000555829.5:c.225-1433G>A (ENTPD5)
ENST00000556299.1:n.602C>T (COQ6)
ENST00000556588.5:n.2991C>T (COQ6)
ENST00000557325.5:c.1201-3430G>A (ENTPD5)	ENSP00000451810.1:n.1201-3430G>A
ENST00000557780.5:n.357C>T (COQ6)
ENST00000629426.2:c.1166C>T (COQ6)	ENSP00000486650.1:p.Ala389Val
NM_182476.2:c.1391C>T (COQ6)	NP_872282.1:p.Ala464Val
NM_182480.2:c.1316C>T (COQ6)	NP_872286.2:p.Ala439Val
XM_005267716.1:c.1226C>T (COQ6)	XP_005267773.1:p.Ala409Val
XM_006720156.1:c.1064C>T (COQ6)	XP_006720219.1:p.Ala355Val
XM_006720325.2:c.1201-3430G>A (ENTPD5)	XP_006720388.1:n.1201-3430G>A
XM_011536807.1:c.1283C>T (COQ6)	XP_011535109.1:p.Ala428Val
XM_011536808.1:c.1166C>T (COQ6)	XP_011535110.1:p.Ala389Val
XM_011536809.1:c.1166C>T (COQ6)	XP_011535111.1:p.Ala389Val
XM_011536810.1:c.905C>T (COQ6)	XP_011535112.1:p.Ala302Val
XM_011536811.1:c.851C>T (COQ6)	XP_011535113.1:p.Ala284Val
NM_001321984.1:c.1201-1433G>A (ENTPD5)	NP_001308913.1:n.1201-1433G>A
NM_001330189.1:c.1201-3430G>A (ENTPD5)	NP_001317118.1:n.1201-3430G>A
XM_006720325.3:c.1201-3430G>A (ENTPD5)	XP_006720388.1:n.1201-3430G>A
XM_011536807.2:c.1283C>T (COQ6)	XP_011535109.1:p.Ala428Val
XM_011536808.2:c.1166C>T (COQ6)	XP_011535110.1:p.Ala389Val
XM_011536809.3:c.1166C>T (COQ6)	XP_011535111.1:p.Ala389Val
XM_011536810.3:c.905C>T (COQ6)	XP_011535112.1:p.Ala302Val
XM_017021351.2:c.851C>T (COQ6)	XP_016876840.1:p.Ala284Val
XM_017021352.2:c.785C>T (COQ6)	XP_016876841.1:p.Ala262Val
XM_017021814.1:c.1201-3430G>A (ENTPD5)	XP_016877303.1:n.1201-3430G>A
XM_017021817.1:c.1060-3430G>A (ENTPD5)	XP_016877306.1:n.1060-3430G>A
XM_024449619.1:c.785C>T (COQ6)	XP_024305387.1:p.Ala262Val
XR_001750342.1:n.1545C>T (COQ6)
NM_001249.4:c.*3945G>A (ENTPD5)	NP_001240.1:n.*3945G>A
NM_001321984.2:c.1201-1433G>A (ENTPD5)	NP_001308913.1:n.1201-1433G>A
NM_001321985.2:c.*3945G>A (ENTPD5)	NP_001308914.1:n.*3945G>A
NM_001321986.2:c.*3945G>A (ENTPD5)	NP_001308915.1:n.*3945G>A
NM_001321987.2:c.*3945G>A (ENTPD5)	NP_001308916.1:n.*3945G>A
NM_001321988.2:c.*3945G>A (ENTPD5)	NP_001308917.1:n.*3945G>A
NM_001330189.2:c.1201-3430G>A (ENTPD5)	NP_001317118.1:n.1201-3430G>A
NM_182476.3:c.1391C>T (COQ6) MANE Select	NP_872282.1:p.Ala464Val
NM_001382258.1:c.1200+7027G>A (ENTPD5)	NP_001369187.1:n.1200+7027G>A
NM_001382259.1:c.1201-3430G>A (ENTPD5)	NP_001369188.1:n.1201-3430G>A
NM_001382260.1:c.1201-3430G>A (ENTPD5)	NP_001369189.1:n.1201-3430G>A
NM_001382262.1:c.1200+7027G>A (ENTPD5)	NP_001369191.1:n.1200+7027G>A
NM_182480.3:c.1316C>T (COQ6)	NP_872286.2:p.Ala439Val