Canonical Allele Identifier: CA1955123368
Gene: ABCC8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17395915G= , CM000673.2:g.17395915G= GRCh38
NC_000011.9:g.17417462G= , CM000673.1:g.17417462G= GRCh37
NC_000011.8:g.17374038G= NCBI36
NG_008867.1:g.85988C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000524561.2:n.3736C=
ENST00000528374.2:c.726C=
ENST00000529967.6:n.2474C=
ENST00000532220.2:n.3368C=
ENST00000642611.2:n.5335C=
ENST00000644057.2:n.578C=
ENST00000645004.2:n.1634C=
ENST00000682051.1:n.4297C=
ENST00000682110.1:n.4350C=
ENST00000682140.1:c.4001C= ENSP00000507829.1:p.Pro1334=
ENST00000682185.1:n.5440C=
ENST00000682204.1:c.*2273C= ENSP00000507094.1:n.*2273C=
ENST00000682215.1:n.4717C=
ENST00000682288.1:c.*2566C= ENSP00000507506.1:n.*2566C=
ENST00000682442.1:n.4570C=
ENST00000682528.1:n.4427C=
ENST00000682673.1:n.4294C=
ENST00000682805.1:n.4755C=
ENST00000682965.1:c.*557C= ENSP00000508229.1:n.*557C=
ENST00000683093.1:n.5434C=
ENST00000683136.1:c.4018C= ENSP00000507768.1:p.Arg1340=
ENST00000683153.1:n.4392C=
ENST00000683365.1:n.4452C=
ENST00000683377.1:n.4350C=
ENST00000683456.1:c.*1272C= ENSP00000508318.1:n.*1272C=
ENST00000683522.1:n.4350C=
ENST00000683562.1:c.*2304C= ENSP00000508265.1:n.*2304C=
ENST00000683693.1:n.5782C=
ENST00000683725.1:c.4135C= ENSP00000507496.1:p.Arg1379=
ENST00000684010.1:n.4345C=
ENST00000684157.1:n.5335C=
ENST00000684253.1:n.4253C=
ENST00000684288.1:c.*2307C= ENSP00000507143.1:n.*2307C=
ENST00000684313.1:n.3782C=
ENST00000684332.1:n.4423C=
ENST00000684371.1:n.4456C=
ENST00000684404.1:n.5378C=
ENST00000684442.1:n.4574C=
ENST00000684555.1:c.*2347C= ENSP00000507705.1:n.*2347C=
ENST00000684571.1:c.3976C= ENSP00000506935.1:p.Arg1326=
ENST00000684593.1:c.*3840C= ENSP00000507005.1:n.*3840C=
ENST00000684711.1:c.*2531C= ENSP00000506841.1:n.*2531C=
ENST00000302539.9:c.4138C= ENSP00000303960.4:p.Arg1380=
ENST00000389817.8:c.4135C= MANE Select ENSP00000374467.4:p.Arg1379=
ENST00000642271.1:c.4132C= ENSP00000493749.1:p.Arg1378=
ENST00000642579.1:c.2189C=
ENST00000642611.1:n.5220C=
ENST00000642902.1:c.3917C=
ENST00000643260.1:c.4135C= ENSP00000494450.1:p.Arg1379=
ENST00000643562.1:c.*2257C= ENSP00000496124.1:n.*2257C=
ENST00000643925.1:c.2775C=
ENST00000644057.1:n.212C=
ENST00000644484.1:c.*3521C= ENSP00000493558.1:n.*3521C=
ENST00000644675.1:c.*2307C= ENSP00000494567.1:n.*2307C=
ENST00000644757.1:c.*3202+349C= ENSP00000495085.1:n.*3202+349C=
ENST00000644772.1:c.4201C= ENSP00000494321.1:p.Arg1401=
ENST00000645004.1:n.1828C=
ENST00000645076.1:c.3334C=
ENST00000645417.1:c.1323C=
ENST00000645744.1:c.*3900C= ENSP00000494564.1:n.*3900C=
ENST00000645760.1:c.4556C=
ENST00000645884.1:c.*1418C= ENSP00000495516.1:n.*1418C=
ENST00000646003.1:c.*2237C= ENSP00000495259.1:n.*2237C=
ENST00000646207.1:c.*2972C= ENSP00000495025.1:n.*2972C=
ENST00000646276.1:c.*3539C= ENSP00000496070.1:n.*3539C=
ENST00000646592.1:c.3441C=
ENST00000646902.1:c.4102C= ENSP00000494101.1:p.Arg1368=
ENST00000646993.1:c.*2677C= ENSP00000493720.1:n.*2677C=
ENST00000647013.1:c.4141C= ENSP00000496741.1:n.4141C=
ENST00000647015.1:c.3886C= ENSP00000495389.1:p.Arg1296=
ENST00000647086.1:c.*3721C= ENSP00000493677.1:n.*3721C=
ENST00000647158.1:c.*2422C= ENSP00000495744.1:n.*2422C=
ENST00000302539.8:c.4138C= ENSP00000303960.4:p.Arg1380=
ENST00000389817.7:c.4135C= ENSP00000374467.3:p.Arg1379=
ENST00000525022.1:n.1C=
ENST00000526168.5:c.3C=
ENST00000532220.1:n.609C=
NM_000352.4:c.4135C= NP_000343.2:p.Arg1379=
NM_001287174.1:c.4138C= NP_001274103.1:p.Arg1380=
XM_011520331.1:c.4135C= XP_011518633.1:p.Arg1379=
XM_011520332.1:c.4138C= XP_011518634.1:p.Arg1380=
XM_011520333.1:c.2635C= XP_011518635.1:p.Arg879=
XR_930890.1:n.4201C=
NM_001351295.1:c.4201C= NP_001338224.1:p.Arg1401=
NM_001351296.1:c.4135C= NP_001338225.1:p.Arg1379=
NM_001351297.1:c.4132C= NP_001338226.1:p.Arg1378=
NR_147094.1:n.4430C=
XM_017018197.2:c.4204C= XP_016873686.1:p.Arg1402=
XM_017018199.1:c.4201C= XP_016873688.1:p.Arg1401=
XM_017018201.2:c.4204C= XP_016873690.1:p.Arg1402=
XM_017018202.1:c.2701C= XP_016873691.1:p.Arg901=
XM_017018204.1:c.2092C= XP_016873693.1:p.Arg698=
XM_024448668.1:c.2503C= XP_024304436.1:p.Arg835=
XR_001747945.2:n.4276C=
XR_001747946.2:n.4207C=
XR_002957189.1:n.5857C=
NM_000352.6:c.4135C= MANE Select NP_000343.2:p.Arg1379=
NM_001287174.2:c.4138C= NP_001274103.1:p.Arg1380=
NM_001351295.2:c.4201C= NP_001338224.1:p.Arg1401=
NM_001351296.2:c.4135C= NP_001338225.1:p.Arg1379=
NM_001351297.2:c.4132C= NP_001338226.1:p.Arg1378=
NR_147094.2:n.4430C=
NM_001287174.3:c.4138C= NP_001274103.1:p.Arg1380=