Canonical Allele Identifier: CA1955128544
Gene: ABCC8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17406782T= , CM000673.2:g.17406782T= GRCh38
NC_000011.9:g.17428329T= , CM000673.1:g.17428329T= GRCh37
NC_000011.8:g.17384905T= NCBI36
NG_008867.1:g.75121A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000524561.2:n.2738A=
ENST00000529967.6:n.1508A=
ENST00000532220.2:n.901A=
ENST00000642611.2:n.3238A=
ENST00000645004.2:n.668A=
ENST00000682051.1:n.3185A=
ENST00000682110.1:n.3238A=
ENST00000682140.1:c.3166A= ENSP00000507829.1:p.Thr1056=
ENST00000682185.1:n.4474A=
ENST00000682204.1:c.*1307A= ENSP00000507094.1:n.*1307A=
ENST00000682215.1:n.3235A=
ENST00000682288.1:c.*1600A= ENSP00000507506.1:n.*1600A=
ENST00000682442.1:n.3458A=
ENST00000682528.1:n.3315A=
ENST00000682673.1:n.3182A=
ENST00000682805.1:n.3235A=
ENST00000682965.1:c.3166A= ENSP00000508229.1:p.Thr1056=
ENST00000683093.1:n.3337A=
ENST00000683136.1:c.3166A= ENSP00000507768.1:p.Thr1056=
ENST00000683153.1:n.3394A=
ENST00000683365.1:n.3340A=
ENST00000683377.1:n.3238A=
ENST00000683456.1:c.*306A= ENSP00000508318.1:n.*306A=
ENST00000683522.1:n.3238A=
ENST00000683562.1:c.*1338A= ENSP00000508265.1:n.*1338A=
ENST00000683693.1:n.3315A=
ENST00000683725.1:c.3169A= ENSP00000507496.1:p.Thr1057=
ENST00000684010.1:n.3233A=
ENST00000684157.1:n.3238A=
ENST00000684253.1:n.3141A=
ENST00000684288.1:c.*1341A= ENSP00000507143.1:n.*1341A=
ENST00000684313.1:n.2670A=
ENST00000684332.1:n.3311A=
ENST00000684371.1:n.3344A=
ENST00000684404.1:n.3281A=
ENST00000684442.1:n.3238A=
ENST00000684555.1:c.*1381A= ENSP00000507705.1:n.*1381A=
ENST00000684571.1:c.3010A= ENSP00000506935.1:p.Thr1004=
ENST00000684593.1:c.*2874A= ENSP00000507005.1:n.*2874A=
ENST00000684711.1:c.*1565A= ENSP00000506841.1:n.*1565A=
ENST00000302539.9:c.3172A= ENSP00000303960.4:p.Thr1058=
ENST00000389817.8:c.3169A= MANE Select ENSP00000374467.4:p.Thr1057=
ENST00000642271.1:c.3166A= ENSP00000493749.1:p.Thr1056=
ENST00000642579.1:c.1253A=
ENST00000642611.1:n.3123A=
ENST00000642902.1:c.2951A=
ENST00000643260.1:c.3169A= ENSP00000494450.1:p.Thr1057=
ENST00000643562.1:c.*1145A= ENSP00000496124.1:n.*1145A=
ENST00000643925.1:c.1293A=
ENST00000644447.1:c.1525A= ENSP00000496282.1:p.Thr509=
ENST00000644484.1:c.*1424A= ENSP00000493558.1:n.*1424A=
ENST00000644542.1:c.*2973A= ENSP00000495532.1:n.*2973A=
ENST00000644675.1:c.*1341A= ENSP00000494567.1:n.*1341A=
ENST00000644757.1:c.*1454A= ENSP00000495085.1:n.*1454A=
ENST00000644772.1:c.3235A= ENSP00000494321.1:p.Thr1079=
ENST00000645004.1:n.308A=
ENST00000645076.1:c.2368A=
ENST00000645417.1:c.335A=
ENST00000645744.1:c.*1433A= ENSP00000494564.1:n.*1433A=
ENST00000645760.1:c.3444A=
ENST00000645884.1:c.*306A= ENSP00000495516.1:n.*306A=
ENST00000646003.1:c.*1125A= ENSP00000495259.1:n.*1125A=
ENST00000646207.1:c.*1636A= ENSP00000495025.1:n.*1636A=
ENST00000646276.1:c.*1442A= ENSP00000496070.1:n.*1442A=
ENST00000646592.1:c.2475A=
ENST00000646902.1:c.3166A= ENSP00000494101.1:p.Thr1056=
ENST00000646993.1:c.*1565A= ENSP00000493720.1:n.*1565A=
ENST00000647013.1:c.3175A= ENSP00000496741.1:n.3175A=
ENST00000647015.1:c.2920A= ENSP00000495389.1:p.Thr974=
ENST00000647086.1:c.*2899A= ENSP00000493677.1:n.*2899A=
ENST00000647158.1:c.*1310A= ENSP00000495744.1:n.*1310A=
ENST00000302539.8:c.3172A= ENSP00000303960.4:p.Thr1058=
ENST00000389817.7:c.3169A= ENSP00000374467.3:p.Thr1057=
ENST00000524561.1:n.301A=
ENST00000526921.5:n.853A=
ENST00000527905.5:c.*45A= ENSP00000431653.1:n.*45A=
NM_000352.4:c.3169A= NP_000343.2:p.Thr1057=
NM_001287174.1:c.3172A= NP_001274103.1:p.Thr1058=
XM_011520331.1:c.3169A= XP_011518633.1:p.Thr1057=
XM_011520332.1:c.3172A= XP_011518634.1:p.Thr1058=
XM_011520333.1:c.1669A= XP_011518635.1:p.Thr557=
XR_930890.1:n.3235A=
XR_930891.1:n.3235A=
XR_930892.1:n.3135A=
XR_930893.1:n.3132A=
NM_001351295.1:c.3235A= NP_001338224.1:p.Thr1079=
NM_001351296.1:c.3169A= NP_001338225.1:p.Thr1057=
NM_001351297.1:c.3166A= NP_001338226.1:p.Thr1056=
NR_147094.1:n.3318A=
XM_017018197.2:c.3238A= XP_016873686.1:p.Thr1080=
XM_017018199.1:c.3235A= XP_016873688.1:p.Thr1079=
XM_017018201.2:c.3238A= XP_016873690.1:p.Thr1080=
XM_017018202.1:c.1735A= XP_016873691.1:p.Thr579=
XM_017018204.1:c.1126A= XP_016873693.1:p.Thr376=
XM_024448668.1:c.1537A= XP_024304436.1:p.Thr513=
XR_001747945.2:n.3310A=
XR_001747946.2:n.3241A=
XR_002957189.1:n.3390A=
NM_000352.6:c.3169A= MANE Select NP_000343.2:p.Thr1057=
NM_001287174.2:c.3172A= NP_001274103.1:p.Thr1058=
NM_001351295.2:c.3235A= NP_001338224.1:p.Thr1079=
NM_001351296.2:c.3169A= NP_001338225.1:p.Thr1057=
NM_001351297.2:c.3166A= NP_001338226.1:p.Thr1056=
NR_147094.2:n.3318A=
NM_001287174.3:c.3172A= NP_001274103.1:p.Thr1058=