Canonical Allele Identifier: CA1955123356
Gene: ABCC8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17395893G= , CM000673.2:g.17395893G= GRCh38
NC_000011.9:g.17417440G= , CM000673.1:g.17417440G= GRCh37
NC_000011.8:g.17374016G= NCBI36
NG_008867.1:g.86010C=

Transcript Alleles

HGVS Amino-acid change
ENST00000524561.2:n.3758C=
ENST00000528374.2:c.748C=
ENST00000529967.6:n.2496C=
ENST00000532220.2:n.3390C=
ENST00000642611.2:n.5357C=
ENST00000644057.2:n.600C=
ENST00000645004.2:n.1656C=
ENST00000682051.1:n.4319C=
ENST00000682110.1:n.4372C=
ENST00000682140.1:c.4023C= ENSP00000507829.1:p.Leu1341=
ENST00000682185.1:n.5462C=
ENST00000682204.1:c.*2295C= ENSP00000507094.1:n.*2295C=
ENST00000682215.1:n.4739C=
ENST00000682288.1:c.*2588C= ENSP00000507506.1:n.*2588C=
ENST00000682442.1:n.4592C=
ENST00000682528.1:n.4449C=
ENST00000682673.1:n.4316C=
ENST00000682805.1:n.4777C=
ENST00000682965.1:c.*579C= ENSP00000508229.1:n.*579C=
ENST00000683093.1:n.5456C=
ENST00000683136.1:c.4040C= ENSP00000507768.1:p.Ser1347=
ENST00000683153.1:n.4414C=
ENST00000683365.1:n.4474C=
ENST00000683377.1:n.4372C=
ENST00000683456.1:c.*1294C= ENSP00000508318.1:n.*1294C=
ENST00000683522.1:n.4372C=
ENST00000683562.1:c.*2326C= ENSP00000508265.1:n.*2326C=
ENST00000683693.1:n.5804C=
ENST00000683725.1:c.4157C= ENSP00000507496.1:p.Ser1386=
ENST00000684010.1:n.4367C=
ENST00000684157.1:n.5357C=
ENST00000684253.1:n.4275C=
ENST00000684288.1:c.*2329C= ENSP00000507143.1:n.*2329C=
ENST00000684313.1:n.3804C=
ENST00000684332.1:n.4445C=
ENST00000684371.1:n.4478C=
ENST00000684404.1:n.5400C=
ENST00000684442.1:n.4596C=
ENST00000684555.1:c.*2369C= ENSP00000507705.1:n.*2369C=
ENST00000684571.1:c.3998C= ENSP00000506935.1:p.Ser1333=
ENST00000684593.1:c.*3862C= ENSP00000507005.1:n.*3862C=
ENST00000684711.1:c.*2553C= ENSP00000506841.1:n.*2553C=
ENST00000302539.9:c.4160C= ENSP00000303960.4:p.Ser1387=
ENST00000389817.8:c.4157C= MANE Select ENSP00000374467.4:p.Ser1386=
ENST00000642271.1:c.4154C= ENSP00000493749.1:p.Ser1385=
ENST00000642579.1:c.2211C=
ENST00000642611.1:n.5242C=
ENST00000642902.1:c.3939C=
ENST00000643260.1:c.4157C= ENSP00000494450.1:p.Ser1386=
ENST00000643562.1:c.*2279C= ENSP00000496124.1:n.*2279C=
ENST00000643925.1:c.2797C=
ENST00000644057.1:n.234C=
ENST00000644484.1:c.*3543C= ENSP00000493558.1:n.*3543C=
ENST00000644675.1:c.*2329C= ENSP00000494567.1:n.*2329C=
ENST00000644757.1:c.*3202+371C= ENSP00000495085.1:n.*3202+371C=
ENST00000644772.1:c.4223C= ENSP00000494321.1:p.Ser1408=
ENST00000645004.1:n.1850C=
ENST00000645076.1:c.3356C=
ENST00000645417.1:c.1345C=
ENST00000645744.1:c.*3922C= ENSP00000494564.1:n.*3922C=
ENST00000645760.1:c.4578C=
ENST00000645884.1:c.*1440C= ENSP00000495516.1:n.*1440C=
ENST00000646003.1:c.*2259C= ENSP00000495259.1:n.*2259C=
ENST00000646207.1:c.*2994C= ENSP00000495025.1:n.*2994C=
ENST00000646276.1:c.*3561C= ENSP00000496070.1:n.*3561C=
ENST00000646592.1:c.3463C=
ENST00000646902.1:c.4124C= ENSP00000494101.1:p.Ser1375=
ENST00000646993.1:c.*2699C= ENSP00000493720.1:n.*2699C=
ENST00000647013.1:c.4163C= ENSP00000496741.1:n.4163C=
ENST00000647015.1:c.3908C= ENSP00000495389.1:p.Ser1303=
ENST00000647086.1:c.*3743C= ENSP00000493677.1:n.*3743C=
ENST00000647158.1:c.*2444C= ENSP00000495744.1:n.*2444C=
ENST00000302539.8:c.4160C= ENSP00000303960.4:p.Ser1387=
ENST00000389817.7:c.4157C= ENSP00000374467.3:p.Ser1386=
ENST00000525022.1:n.23C=
ENST00000526168.5:c.25C=
NM_000352.4:c.4157C= NP_000343.2:p.Ser1386=
NM_001287174.1:c.4160C= NP_001274103.1:p.Ser1387=
XM_011520331.1:c.4157C= XP_011518633.1:p.Ser1386=
XM_011520332.1:c.4160C= XP_011518634.1:p.Ser1387=
XM_011520333.1:c.2657C= XP_011518635.1:p.Ser886=
XR_930890.1:n.4223C=
NM_001351295.1:c.4223C= NP_001338224.1:p.Ser1408=
NM_001351296.1:c.4157C= NP_001338225.1:p.Ser1386=
NM_001351297.1:c.4154C= NP_001338226.1:p.Ser1385=
NR_147094.1:n.4452C=
XM_017018197.2:c.4226C= XP_016873686.1:p.Ser1409=
XM_017018199.1:c.4223C= XP_016873688.1:p.Ser1408=
XM_017018201.2:c.4226C= XP_016873690.1:p.Ser1409=
XM_017018202.1:c.2723C= XP_016873691.1:p.Ser908=
XM_017018204.1:c.2114C= XP_016873693.1:p.Ser705=
XM_024448668.1:c.2525C= XP_024304436.1:p.Ser842=
XR_001747945.2:n.4298C=
XR_001747946.2:n.4229C=
XR_002957189.1:n.5879C=
NM_000352.6:c.4157C= MANE Select NP_000343.2:p.Ser1386=
NM_001287174.2:c.4160C= NP_001274103.1:p.Ser1387=
NM_001351295.2:c.4223C= NP_001338224.1:p.Ser1408=
NM_001351296.2:c.4157C= NP_001338225.1:p.Ser1386=
NM_001351297.2:c.4154C= NP_001338226.1:p.Ser1385=
NR_147094.2:n.4452C=
NM_001287174.3:c.4160C= NP_001274103.1:p.Ser1387=