Canonical Allele Identifier: CA1955129305
Gene: ABCC8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17408513A= , CM000673.2:g.17408513A= GRCh38
NC_000011.9:g.17430060A= , CM000673.1:g.17430060A= GRCh37
NC_000011.8:g.17386636A= NCBI36
NG_008867.1:g.73390T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000524561.2:n.2368T=
ENST00000529967.6:n.958T=
ENST00000532220.2:n.431T=
ENST00000642611.2:n.2768T=
ENST00000682051.1:n.2715T=
ENST00000682110.1:n.2768T=
ENST00000682140.1:c.2696T= ENSP00000507829.1:p.Ile899=
ENST00000682185.1:n.4004T=
ENST00000682204.1:c.*837T= ENSP00000507094.1:n.*837T=
ENST00000682215.1:n.2765T=
ENST00000682288.1:c.*1130T= ENSP00000507506.1:n.*1130T=
ENST00000682442.1:n.2889T=
ENST00000682528.1:n.2765T=
ENST00000682673.1:n.2712T=
ENST00000682805.1:n.2765T=
ENST00000682965.1:c.2696T= ENSP00000508229.1:p.Ile899=
ENST00000683093.1:n.2867T=
ENST00000683136.1:c.2696T= ENSP00000507768.1:p.Ile899=
ENST00000683153.1:n.2924T=
ENST00000683365.1:n.2870T=
ENST00000683377.1:n.2768T=
ENST00000683456.1:c.2699T= ENSP00000508318.1:p.Ile900=
ENST00000683522.1:n.2768T=
ENST00000683562.1:c.*868T= ENSP00000508265.1:n.*868T=
ENST00000683693.1:n.2765T=
ENST00000683725.1:c.2699T= ENSP00000507496.1:p.Ile900=
ENST00000684010.1:n.2683T=
ENST00000684157.1:n.2768T=
ENST00000684253.1:n.2671T=
ENST00000684288.1:c.*871T= ENSP00000507143.1:n.*871T=
ENST00000684313.1:n.2200T=
ENST00000684332.1:n.2841T=
ENST00000684371.1:n.2874T=
ENST00000684404.1:n.2765T=
ENST00000684442.1:n.2768T=
ENST00000684555.1:c.*911T= ENSP00000507705.1:n.*911T=
ENST00000684571.1:c.2540T= ENSP00000506935.1:p.Ile847=
ENST00000684593.1:c.*2404T= ENSP00000507005.1:n.*2404T=
ENST00000684711.1:c.*1095T= ENSP00000506841.1:n.*1095T=
ENST00000302539.9:c.2702T= ENSP00000303960.4:p.Ile901=
ENST00000389817.8:c.2699T= MANE Select ENSP00000374467.4:p.Ile900=
ENST00000642271.1:c.2696T= ENSP00000493749.1:p.Ile899=
ENST00000642579.1:c.783T=
ENST00000642611.1:n.2653T=
ENST00000642902.1:c.2534T=
ENST00000643260.1:c.2699T= ENSP00000494450.1:p.Ile900=
ENST00000643562.1:c.*675T= ENSP00000496124.1:n.*675T=
ENST00000643925.1:c.743T=
ENST00000644447.1:c.1055T= ENSP00000496282.1:p.Ile352=
ENST00000644472.1:c.*1060T= ENSP00000495378.1:n.*1060T=
ENST00000644484.1:c.*908T= ENSP00000493558.1:n.*908T=
ENST00000644542.1:c.*2404T= ENSP00000495532.1:n.*2404T=
ENST00000644675.1:c.*871T= ENSP00000494567.1:n.*871T=
ENST00000644757.1:c.*1004T= ENSP00000495085.1:n.*1004T=
ENST00000644772.1:c.2765T= ENSP00000494321.1:p.Ile922=
ENST00000645076.1:c.1951T=
ENST00000645744.1:c.*1063T= ENSP00000494564.1:n.*1063T=
ENST00000645760.1:c.2974T=
ENST00000645884.1:c.2699T= ENSP00000495516.1:p.Ile900=
ENST00000646003.1:c.*755T= ENSP00000495259.1:n.*755T=
ENST00000646207.1:c.*1063T= ENSP00000495025.1:n.*1063T=
ENST00000646276.1:c.*972T= ENSP00000496070.1:n.*972T=
ENST00000646592.1:c.1925T=
ENST00000646902.1:c.2696T= ENSP00000494101.1:p.Ile899=
ENST00000646993.1:c.*1095T= ENSP00000493720.1:n.*1095T=
ENST00000647013.1:c.2705T= ENSP00000496741.1:n.2705T=
ENST00000647015.1:c.2450T= ENSP00000495389.1:p.Ile817=
ENST00000647086.1:c.*2429T= ENSP00000493677.1:n.*2429T=
ENST00000647158.1:c.*840T= ENSP00000495744.1:n.*840T=
ENST00000302539.8:c.2702T= ENSP00000303960.4:p.Ile901=
ENST00000389817.7:c.2699T= ENSP00000374467.3:p.Ile900=
ENST00000526921.5:n.383T=
ENST00000527905.5:c.2669T= ENSP00000431653.1:p.Ile890=
ENST00000529967.5:n.368T=
NM_000352.4:c.2699T= NP_000343.2:p.Ile900=
NM_001287174.1:c.2702T= NP_001274103.1:p.Ile901=
XM_011520331.1:c.2699T= XP_011518633.1:p.Ile900=
XM_011520332.1:c.2702T= XP_011518634.1:p.Ile901=
XM_011520333.1:c.1199T= XP_011518635.1:p.Ile400=
XM_011520334.1:c.2702T= XP_011518636.1:p.Ile901=
XR_930890.1:n.2765T=
XR_930891.1:n.2765T=
XR_930892.1:n.2765T=
XR_930893.1:n.2762T=
NM_001351295.1:c.2765T= NP_001338224.1:p.Ile922=
NM_001351296.1:c.2699T= NP_001338225.1:p.Ile900=
NM_001351297.1:c.2696T= NP_001338226.1:p.Ile899=
NR_147094.1:n.2768T=
XM_017018197.2:c.2768T= XP_016873686.1:p.Ile923=
XM_017018199.1:c.2765T= XP_016873688.1:p.Ile922=
XM_017018201.2:c.2768T= XP_016873690.1:p.Ile923=
XM_017018202.1:c.1265T= XP_016873691.1:p.Ile422=
XM_017018204.1:c.656T= XP_016873693.1:p.Ile219=
XM_024448668.1:c.1067T= XP_024304436.1:p.Ile356=
XR_001747945.2:n.2840T=
XR_001747946.2:n.2771T=
XR_002957189.1:n.2840T=
NM_000352.6:c.2699T= MANE Select NP_000343.2:p.Ile900=
NM_001287174.2:c.2702T= NP_001274103.1:p.Ile901=
NM_001351295.2:c.2765T= NP_001338224.1:p.Ile922=
NM_001351296.2:c.2699T= NP_001338225.1:p.Ile900=
NM_001351297.2:c.2696T= NP_001338226.1:p.Ile899=
NR_147094.2:n.2768T=
NM_001287174.3:c.2702T= NP_001274103.1:p.Ile901=