Canonical Allele Identifier: CA2146830791
Community Standard Title: NM_182476.3(COQ6):c.484C= (p.Arg162=)

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.73958149C= , CM000676.2:g.73958149C= GRCh38
NC_000014.8:g.74424852C= , CM000676.1:g.74424852C= GRCh37
NC_000014.7:g.73494605C= NCBI36
NG_032805.1:g.13216C=

Transcript Alleles

HGVS Amino-acid Change
NM_182476.3:c.484C= (COQ6) MANE Select NP_872282.1:p.Arg162=
ENST00000334571.7:c.484C= (COQ6) MANE Select ENSP00000333946.2:p.Arg162=
NM_001330189.1:c.*1381G= (ENTPD5) NP_001317118.1:n.*1381G=
NM_001330189.2:c.*1381G= (ENTPD5) NP_001317118.1:n.*1381G=
NM_001382258.1:c.1201-2562G= (ENTPD5) NP_001369187.1:n.1201-2562G=
NM_001382259.1:c.*1381G= (ENTPD5) NP_001369188.1:n.*1381G=
NM_001382260.1:c.*1381G= (ENTPD5) NP_001369189.1:n.*1381G=
NM_001382262.1:c.1201-2321G= (ENTPD5) NP_001369191.1:n.1201-2321G=
NM_182476.2:c.484C= (COQ6) NP_872282.1:p.Arg162=
NM_182480.2:c.409C= (COQ6) NP_872286.2:p.Arg137=
NM_182480.3:c.409C= (COQ6) NP_872286.2:p.Arg137=
ENST00000238709.8:c.481C= (COQ6) ENSP00000238709.5:p.Arg161=
ENST00000334571.6:c.484C= (COQ6) ENSP00000333946.2:p.Arg162=
ENST00000394026.8:c.409C= (COQ6) ENSP00000377594.4:p.Arg137=
ENST00000553462.6:n.332C= (COQ6)
ENST00000554153.5:c.*89C= (COQ6) ENSP00000451685.1:n.*89C=
ENST00000554320.1:c.259C= (COQ6) ENSP00000451123.1:p.Arg87=
ENST00000554341.6:c.*89C= (COQ6) ENSP00000450736.2:n.*89C=
ENST00000554920.5:c.481+2221C= (COQ6) ENSP00000451562.1:n.481+2221C=
ENST00000555511.5:n.602C= (COQ6)
ENST00000556300.6:n.518C= (COQ6)
ENST00000557205.6:n.448C= (COQ6)
ENST00000557325.5:c.*1381G= (ENTPD5) ENSP00000451810.1:n.*1381G=
ENST00000557584.5:c.*89C= (COQ6) ENSP00000450511.1:n.*89C=
ENST00000629426.2:c.259C= (COQ6) ENSP00000486650.1:p.Arg87=
XM_005267716.1:c.319C= (COQ6) XP_005267773.1:p.Arg107=
XM_006720156.1:c.157C= (COQ6) XP_006720219.1:p.Arg53=
XM_011536807.1:c.484C= (COQ6) XP_011535109.1:p.Arg162=
XM_011536807.2:c.484C= (COQ6) XP_011535109.1:p.Arg162=
XM_011536808.1:c.259C= (COQ6) XP_011535110.1:p.Arg87=
XM_011536808.2:c.259C= (COQ6) XP_011535110.1:p.Arg87=
XM_011536809.1:c.259C= (COQ6) XP_011535111.1:p.Arg87=
XM_011536809.3:c.259C= (COQ6) XP_011535111.1:p.Arg87=
XM_011536810.1:c.484C= (COQ6) XP_011535112.1:p.Arg162=
XM_011536810.3:c.484C= (COQ6) XP_011535112.1:p.Arg162=
XM_011536811.1:c.73-822C= (COQ6) XP_011535113.1:n.73-822C=
XM_017021351.2:c.73-822C= (COQ6) XP_016876840.1:n.73-822C=
XM_017021352.2:c.-816C= (COQ6) XP_016876841.1:n.-816C=
XM_024449619.1:c.-265C= (COQ6) XP_024305387.1:n.-265C=
XR_001750342.1:n.448C= (COQ6)
XR_943465.1:n.537C= (COQ6)
XR_943465.3:n.514C= (COQ6)
XR_943466.1:n.537C= (COQ6)
XR_943466.3:n.514C= (COQ6)