Canonical Allele Identifier: CA1955123348
Gene: ABCC8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17395874G= , CM000673.2:g.17395874G= GRCh38
NC_000011.9:g.17417421G= , CM000673.1:g.17417421G= GRCh37
NC_000011.8:g.17373997G= NCBI36
NG_008867.1:g.86029C=

Transcript Alleles

HGVS Amino-acid change
ENST00000524561.2:n.3777C=
ENST00000528374.2:c.767C=
ENST00000529967.6:n.2515C=
ENST00000532220.2:n.3409C=
ENST00000642611.2:n.5376C=
ENST00000644057.2:n.619C=
ENST00000645004.2:n.1675C=
ENST00000682051.1:n.4338C=
ENST00000682110.1:n.4391C=
ENST00000682140.1:c.4042C= ENSP00000507829.1:p.Pro1348=
ENST00000682185.1:n.5481C=
ENST00000682204.1:c.*2314C= ENSP00000507094.1:n.*2314C=
ENST00000682215.1:n.4758C=
ENST00000682288.1:c.*2607C= ENSP00000507506.1:n.*2607C=
ENST00000682442.1:n.4611C=
ENST00000682528.1:n.4468C=
ENST00000682673.1:n.4335C=
ENST00000682805.1:n.4796C=
ENST00000682965.1:c.*598C= ENSP00000508229.1:n.*598C=
ENST00000683093.1:n.5475C=
ENST00000683136.1:c.4059C= ENSP00000507768.1:p.Phe1353=
ENST00000683153.1:n.4433C=
ENST00000683365.1:n.4493C=
ENST00000683377.1:n.4391C=
ENST00000683456.1:c.*1313C= ENSP00000508318.1:n.*1313C=
ENST00000683522.1:n.4391C=
ENST00000683562.1:c.*2345C= ENSP00000508265.1:n.*2345C=
ENST00000683693.1:n.5823C=
ENST00000683725.1:c.4176C= ENSP00000507496.1:p.Phe1392=
ENST00000684010.1:n.4386C=
ENST00000684157.1:n.5376C=
ENST00000684253.1:n.4294C=
ENST00000684288.1:c.*2348C= ENSP00000507143.1:n.*2348C=
ENST00000684313.1:n.3823C=
ENST00000684332.1:n.4464C=
ENST00000684371.1:n.4497C=
ENST00000684404.1:n.5419C=
ENST00000684442.1:n.4615C=
ENST00000684555.1:c.*2388C= ENSP00000507705.1:n.*2388C=
ENST00000684571.1:c.4017C= ENSP00000506935.1:p.Phe1339=
ENST00000684593.1:c.*3881C= ENSP00000507005.1:n.*3881C=
ENST00000684711.1:c.*2572C= ENSP00000506841.1:n.*2572C=
ENST00000302539.9:c.4179C= ENSP00000303960.4:p.Phe1393=
ENST00000389817.8:c.4176C= MANE Select ENSP00000374467.4:p.Phe1392=
ENST00000642271.1:c.4173C= ENSP00000493749.1:p.Phe1391=
ENST00000642579.1:c.2230C=
ENST00000642611.1:n.5261C=
ENST00000642902.1:c.3958C=
ENST00000643260.1:c.4176C= ENSP00000494450.1:p.Phe1392=
ENST00000643562.1:c.*2298C= ENSP00000496124.1:n.*2298C=
ENST00000643925.1:c.2816C=
ENST00000644057.1:n.253C=
ENST00000644484.1:c.*3562C= ENSP00000493558.1:n.*3562C=
ENST00000644675.1:c.*2348C= ENSP00000494567.1:n.*2348C=
ENST00000644757.1:c.*3202+390C= ENSP00000495085.1:n.*3202+390C=
ENST00000644772.1:c.4242C= ENSP00000494321.1:p.Phe1414=
ENST00000645004.1:n.1869C=
ENST00000645076.1:c.3375C=
ENST00000645417.1:c.1364C=
ENST00000645744.1:c.*3941C= ENSP00000494564.1:n.*3941C=
ENST00000645760.1:c.4597C=
ENST00000645884.1:c.*1459C= ENSP00000495516.1:n.*1459C=
ENST00000646003.1:c.*2278C= ENSP00000495259.1:n.*2278C=
ENST00000646207.1:c.*3013C= ENSP00000495025.1:n.*3013C=
ENST00000646276.1:c.*3580C= ENSP00000496070.1:n.*3580C=
ENST00000646592.1:c.3482C=
ENST00000646902.1:c.4143C= ENSP00000494101.1:p.Phe1381=
ENST00000646993.1:c.*2718C= ENSP00000493720.1:n.*2718C=
ENST00000647013.1:c.4182C= ENSP00000496741.1:n.4182C=
ENST00000647015.1:c.3927C= ENSP00000495389.1:p.Phe1309=
ENST00000647086.1:c.*3762C= ENSP00000493677.1:n.*3762C=
ENST00000647158.1:c.*2463C= ENSP00000495744.1:n.*2463C=
ENST00000302539.8:c.4179C= ENSP00000303960.4:p.Phe1393=
ENST00000389817.7:c.4176C= ENSP00000374467.3:p.Phe1392=
ENST00000525022.1:n.42C=
ENST00000526168.5:c.44C=
ENST00000531642.5:c.12C=
NM_000352.4:c.4176C= NP_000343.2:p.Phe1392=
NM_001287174.1:c.4179C= NP_001274103.1:p.Phe1393=
XM_011520331.1:c.4176C= XP_011518633.1:p.Phe1392=
XM_011520332.1:c.4179C= XP_011518634.1:p.Phe1393=
XM_011520333.1:c.2676C= XP_011518635.1:p.Phe892=
XR_930890.1:n.4242C=
NM_001351295.1:c.4242C= NP_001338224.1:p.Phe1414=
NM_001351296.1:c.4176C= NP_001338225.1:p.Phe1392=
NM_001351297.1:c.4173C= NP_001338226.1:p.Phe1391=
NR_147094.1:n.4471C=
XM_017018197.2:c.4245C= XP_016873686.1:p.Phe1415=
XM_017018199.1:c.4242C= XP_016873688.1:p.Phe1414=
XM_017018201.2:c.4245C= XP_016873690.1:p.Phe1415=
XM_017018202.1:c.2742C= XP_016873691.1:p.Phe914=
XM_017018204.1:c.2133C= XP_016873693.1:p.Phe711=
XM_024448668.1:c.2544C= XP_024304436.1:p.Phe848=
XR_001747945.2:n.4317C=
XR_001747946.2:n.4248C=
XR_002957189.1:n.5898C=
NM_000352.6:c.4176C= MANE Select NP_000343.2:p.Phe1392=
NM_001287174.2:c.4179C= NP_001274103.1:p.Phe1393=
NM_001351295.2:c.4242C= NP_001338224.1:p.Phe1414=
NM_001351296.2:c.4176C= NP_001338225.1:p.Phe1392=
NM_001351297.2:c.4173C= NP_001338226.1:p.Phe1391=
NR_147094.2:n.4471C=
NM_001287174.3:c.4179C= NP_001274103.1:p.Phe1393=