Canonical Allele Identifier: CA1955128496
Gene: ABCC8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17406661T= , CM000673.2:g.17406661T= GRCh38
NC_000011.9:g.17428208T= , CM000673.1:g.17428208T= GRCh37
NC_000011.8:g.17384784T= NCBI36
NG_008867.1:g.75242A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000524561.2:n.2859A=
ENST00000529967.6:n.1629A=
ENST00000532220.2:n.1022A=
ENST00000642611.2:n.3359A=
ENST00000645004.2:n.789A=
ENST00000682051.1:n.3306A=
ENST00000682110.1:n.3359A=
ENST00000682140.1:c.3287A= ENSP00000507829.1:p.His1096=
ENST00000682185.1:n.4595A=
ENST00000682204.1:c.*1428A= ENSP00000507094.1:n.*1428A=
ENST00000682215.1:n.3356A=
ENST00000682288.1:c.*1721A= ENSP00000507506.1:n.*1721A=
ENST00000682442.1:n.3579A=
ENST00000682528.1:n.3436A=
ENST00000682673.1:n.3303A=
ENST00000682805.1:n.3356A=
ENST00000682965.1:c.3287A= ENSP00000508229.1:p.His1096=
ENST00000683093.1:n.3458A=
ENST00000683136.1:c.3287A= ENSP00000507768.1:p.His1096=
ENST00000683153.1:n.3515A=
ENST00000683365.1:n.3461A=
ENST00000683377.1:n.3359A=
ENST00000683456.1:c.*427A= ENSP00000508318.1:n.*427A=
ENST00000683522.1:n.3359A=
ENST00000683562.1:c.*1459A= ENSP00000508265.1:n.*1459A=
ENST00000683693.1:n.3436A=
ENST00000683725.1:c.3290A= ENSP00000507496.1:p.His1097=
ENST00000684010.1:n.3354A=
ENST00000684157.1:n.3359A=
ENST00000684253.1:n.3262A=
ENST00000684288.1:c.*1462A= ENSP00000507143.1:n.*1462A=
ENST00000684313.1:n.2791A=
ENST00000684332.1:n.3432A=
ENST00000684371.1:n.3465A=
ENST00000684404.1:n.3402A=
ENST00000684442.1:n.3359A=
ENST00000684555.1:c.*1502A= ENSP00000507705.1:n.*1502A=
ENST00000684571.1:c.3131A= ENSP00000506935.1:p.His1044=
ENST00000684593.1:c.*2995A= ENSP00000507005.1:n.*2995A=
ENST00000684711.1:c.*1686A= ENSP00000506841.1:n.*1686A=
ENST00000302539.9:c.3293A= ENSP00000303960.4:p.His1098=
ENST00000389817.8:c.3290A= MANE Select ENSP00000374467.4:p.His1097=
ENST00000642271.1:c.3287A= ENSP00000493749.1:p.His1096=
ENST00000642579.1:c.1374A=
ENST00000642611.1:n.3244A=
ENST00000642902.1:c.3072A=
ENST00000643260.1:c.3290A= ENSP00000494450.1:p.His1097=
ENST00000643562.1:c.*1266A= ENSP00000496124.1:n.*1266A=
ENST00000643925.1:c.1414A=
ENST00000644447.1:c.1646A= ENSP00000496282.1:p.His549=
ENST00000644484.1:c.*1545A= ENSP00000493558.1:n.*1545A=
ENST00000644542.1:c.*3094A= ENSP00000495532.1:n.*3094A=
ENST00000644675.1:c.*1462A= ENSP00000494567.1:n.*1462A=
ENST00000644757.1:c.*1575A= ENSP00000495085.1:n.*1575A=
ENST00000644772.1:c.3356A= ENSP00000494321.1:p.His1119=
ENST00000645004.1:n.429A=
ENST00000645076.1:c.2489A=
ENST00000645417.1:c.456A=
ENST00000645744.1:c.*1554A= ENSP00000494564.1:n.*1554A=
ENST00000645760.1:c.3565A=
ENST00000645884.1:c.*427A= ENSP00000495516.1:n.*427A=
ENST00000646003.1:c.*1246A= ENSP00000495259.1:n.*1246A=
ENST00000646207.1:c.*1757A= ENSP00000495025.1:n.*1757A=
ENST00000646276.1:c.*1563A= ENSP00000496070.1:n.*1563A=
ENST00000646592.1:c.2596A=
ENST00000646902.1:c.3287A= ENSP00000494101.1:p.His1096=
ENST00000646993.1:c.*1686A= ENSP00000493720.1:n.*1686A=
ENST00000647013.1:c.3296A= ENSP00000496741.1:n.3296A=
ENST00000647015.1:c.3041A= ENSP00000495389.1:p.His1014=
ENST00000647086.1:c.*3020A= ENSP00000493677.1:n.*3020A=
ENST00000647158.1:c.*1431A= ENSP00000495744.1:n.*1431A=
ENST00000302539.8:c.3293A= ENSP00000303960.4:p.His1098=
ENST00000389817.7:c.3290A= ENSP00000374467.3:p.His1097=
ENST00000524561.1:n.422A=
ENST00000527905.5:c.*166A= ENSP00000431653.1:n.*166A=
NM_000352.4:c.3290A= NP_000343.2:p.His1097=
NM_001287174.1:c.3293A= NP_001274103.1:p.His1098=
XM_011520331.1:c.3290A= XP_011518633.1:p.His1097=
XM_011520332.1:c.3293A= XP_011518634.1:p.His1098=
XM_011520333.1:c.1790A= XP_011518635.1:p.His597=
XR_930890.1:n.3356A=
XR_930891.1:n.3356A=
XR_930892.1:n.3256A=
XR_930893.1:n.3253A=
NM_001351295.1:c.3356A= NP_001338224.1:p.His1119=
NM_001351296.1:c.3290A= NP_001338225.1:p.His1097=
NM_001351297.1:c.3287A= NP_001338226.1:p.His1096=
NR_147094.1:n.3439A=
XM_017018197.2:c.3359A= XP_016873686.1:p.His1120=
XM_017018199.1:c.3356A= XP_016873688.1:p.His1119=
XM_017018201.2:c.3359A= XP_016873690.1:p.His1120=
XM_017018202.1:c.1856A= XP_016873691.1:p.His619=
XM_017018204.1:c.1247A= XP_016873693.1:p.His416=
XM_024448668.1:c.1658A= XP_024304436.1:p.His553=
XR_001747945.2:n.3431A=
XR_001747946.2:n.3362A=
XR_002957189.1:n.3511A=
NM_000352.6:c.3290A= MANE Select NP_000343.2:p.His1097=
NM_001287174.2:c.3293A= NP_001274103.1:p.His1098=
NM_001351295.2:c.3356A= NP_001338224.1:p.His1119=
NM_001351296.2:c.3290A= NP_001338225.1:p.His1097=
NM_001351297.2:c.3287A= NP_001338226.1:p.His1096=
NR_147094.2:n.3439A=
NM_001287174.3:c.3293A= NP_001274103.1:p.His1098=