Canonical Allele Identifier: CA1955123253
Gene: ABCC8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17395687G= , CM000673.2:g.17395687G= GRCh38
NC_000011.9:g.17417234G= , CM000673.1:g.17417234G= GRCh37
NC_000011.8:g.17373810G= NCBI36
NG_008867.1:g.86216C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000524561.2:n.3831C=
ENST00000528374.2:c.821C=
ENST00000529967.6:n.2569C=
ENST00000532220.2:n.3463C=
ENST00000642611.2:n.5563C=
ENST00000644057.2:n.806C=
ENST00000645004.2:n.1729C=
ENST00000682051.1:n.4392C=
ENST00000682110.1:n.4445C=
ENST00000682140.1:c.*16C= ENSP00000507829.1:n.*16C=
ENST00000682185.1:n.5535C=
ENST00000682204.1:c.*2368C= ENSP00000507094.1:n.*2368C=
ENST00000682215.1:n.4812C=
ENST00000682288.1:c.*2661C= ENSP00000507506.1:n.*2661C=
ENST00000682442.1:n.4665C=
ENST00000682528.1:n.4522C=
ENST00000682673.1:n.4389C=
ENST00000682805.1:n.4850C=
ENST00000682965.1:c.*652C= ENSP00000508229.1:n.*652C=
ENST00000683093.1:n.5529C=
ENST00000683136.1:c.4113C= ENSP00000507768.1:p.Ala1371=
ENST00000683153.1:n.4487C=
ENST00000683365.1:n.4547C=
ENST00000683377.1:n.4445C=
ENST00000683456.1:c.*1367C= ENSP00000508318.1:n.*1367C=
ENST00000683522.1:n.4445C=
ENST00000683562.1:c.*2399C= ENSP00000508265.1:n.*2399C=
ENST00000683693.1:n.6010C=
ENST00000683725.1:c.4230C= ENSP00000507496.1:p.Ala1410=
ENST00000684010.1:n.4440C=
ENST00000684157.1:n.5430C=
ENST00000684253.1:n.4348C=
ENST00000684288.1:c.*2402C= ENSP00000507143.1:n.*2402C=
ENST00000684313.1:n.3877C=
ENST00000684332.1:n.4518C=
ENST00000684371.1:n.4551C=
ENST00000684404.1:n.5473C=
ENST00000684442.1:n.4669C=
ENST00000684555.1:c.*2442C= ENSP00000507705.1:n.*2442C=
ENST00000684571.1:c.4071C= ENSP00000506935.1:p.Ala1357=
ENST00000684593.1:c.*3935C= ENSP00000507005.1:n.*3935C=
ENST00000684711.1:c.*2626C= ENSP00000506841.1:n.*2626C=
ENST00000302539.9:c.4233C= ENSP00000303960.4:p.Ala1411=
ENST00000389817.8:c.4230C= MANE Select ENSP00000374467.4:p.Ala1410=
ENST00000642271.1:c.4227C= ENSP00000493749.1:p.Ala1409=
ENST00000642579.1:c.2284C=
ENST00000642611.1:n.5448C=
ENST00000642902.1:c.4012C=
ENST00000643260.1:c.4230C= ENSP00000494450.1:p.Ala1410=
ENST00000643562.1:c.*2352C= ENSP00000496124.1:n.*2352C=
ENST00000643925.1:c.2870C=
ENST00000644057.1:n.307C=
ENST00000644484.1:c.*3616C= ENSP00000493558.1:n.*3616C=
ENST00000644675.1:c.*2402C= ENSP00000494567.1:n.*2402C=
ENST00000644757.1:c.*3202+577C= ENSP00000495085.1:n.*3202+577C=
ENST00000644772.1:c.4296C= ENSP00000494321.1:p.Ala1432=
ENST00000645004.1:n.1923C=
ENST00000645076.1:c.3429C=
ENST00000645417.1:c.1418C=
ENST00000645744.1:c.*3964-49C= ENSP00000494564.1:n.*3964-49C=
ENST00000645760.1:c.4651C=
ENST00000645884.1:c.*1513C= ENSP00000495516.1:n.*1513C=
ENST00000646003.1:c.*2301-49C= ENSP00000495259.1:n.*2301-49C=
ENST00000646207.1:c.*3067C= ENSP00000495025.1:n.*3067C=
ENST00000646276.1:c.*3634C= ENSP00000496070.1:n.*3634C=
ENST00000646592.1:c.3536C=
ENST00000646902.1:c.4197C= ENSP00000494101.1:p.Ala1399=
ENST00000646993.1:c.*2772C= ENSP00000493720.1:n.*2772C=
ENST00000647013.1:c.4236C= ENSP00000496741.1:n.4236C=
ENST00000647015.1:c.3981C= ENSP00000495389.1:p.Ala1327=
ENST00000647086.1:c.*3816C= ENSP00000493677.1:n.*3816C=
ENST00000647158.1:c.*2517C= ENSP00000495744.1:n.*2517C=
ENST00000302539.8:c.4233C= ENSP00000303960.4:p.Ala1411=
ENST00000389817.7:c.4230C= ENSP00000374467.3:p.Ala1410=
ENST00000525022.1:n.229C=
ENST00000526037.5:n.94C=
ENST00000526168.5:c.67-49C=
ENST00000531642.5:c.66C=
NM_000352.4:c.4230C= NP_000343.2:p.Ala1410=
NM_001287174.1:c.4233C= NP_001274103.1:p.Ala1411=
XM_011520331.1:c.4230C= XP_011518633.1:p.Ala1410=
XM_011520332.1:c.4233C= XP_011518634.1:p.Ala1411=
XM_011520333.1:c.2730C= XP_011518635.1:p.Ala910=
XR_930890.1:n.4296C=
NM_001351295.1:c.4296C= NP_001338224.1:p.Ala1432=
NM_001351296.1:c.4230C= NP_001338225.1:p.Ala1410=
NM_001351297.1:c.4227C= NP_001338226.1:p.Ala1409=
NR_147094.1:n.4525C=
XM_017018197.2:c.4299C= XP_016873686.1:p.Ala1433=
XM_017018199.1:c.4296C= XP_016873688.1:p.Ala1432=
XM_017018201.2:c.4299C= XP_016873690.1:p.Ala1433=
XM_017018202.1:c.2796C= XP_016873691.1:p.Ala932=
XM_017018204.1:c.2187C= XP_016873693.1:p.Ala729=
XM_024448668.1:c.2598C= XP_024304436.1:p.Ala866=
XR_001747945.2:n.4371C=
XR_001747946.2:n.4302C=
XR_002957189.1:n.6085C=
NM_000352.6:c.4230C= MANE Select NP_000343.2:p.Ala1410=
NM_001287174.2:c.4233C= NP_001274103.1:p.Ala1411=
NM_001351295.2:c.4296C= NP_001338224.1:p.Ala1432=
NM_001351296.2:c.4230C= NP_001338225.1:p.Ala1410=
NM_001351297.2:c.4227C= NP_001338226.1:p.Ala1409=
NR_147094.2:n.4525C=
NM_001287174.3:c.4233C= NP_001274103.1:p.Ala1411=