Canonical Allele Identifier: CA1955123376
Gene: ABCC8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17395928G= , CM000673.2:g.17395928G= GRCh38
NC_000011.9:g.17417475G= , CM000673.1:g.17417475G= GRCh37
NC_000011.8:g.17374051G= NCBI36
NG_008867.1:g.85975C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000524561.2:n.3723C=
ENST00000528374.2:c.713C=
ENST00000529967.6:n.2461C=
ENST00000532220.2:n.3355C=
ENST00000642611.2:n.5322C=
ENST00000644057.2:n.565C=
ENST00000645004.2:n.1621C=
ENST00000682051.1:n.4284C=
ENST00000682110.1:n.4337C=
ENST00000682140.1:c.3988C= ENSP00000507829.1:p.Arg1330=
ENST00000682185.1:n.5427C=
ENST00000682204.1:c.*2260C= ENSP00000507094.1:n.*2260C=
ENST00000682215.1:n.4704C=
ENST00000682288.1:c.*2553C= ENSP00000507506.1:n.*2553C=
ENST00000682442.1:n.4557C=
ENST00000682528.1:n.4414C=
ENST00000682673.1:n.4281C=
ENST00000682805.1:n.4742C=
ENST00000682965.1:c.*544C= ENSP00000508229.1:n.*544C=
ENST00000683093.1:n.5421C=
ENST00000683136.1:c.4005C= ENSP00000507768.1:p.Ile1335=
ENST00000683153.1:n.4379C=
ENST00000683365.1:n.4439C=
ENST00000683377.1:n.4337C=
ENST00000683456.1:c.*1259C= ENSP00000508318.1:n.*1259C=
ENST00000683522.1:n.4337C=
ENST00000683562.1:c.*2291C= ENSP00000508265.1:n.*2291C=
ENST00000683693.1:n.5769C=
ENST00000683725.1:c.4122C= ENSP00000507496.1:p.Ile1374=
ENST00000684010.1:n.4332C=
ENST00000684157.1:n.5322C=
ENST00000684253.1:n.4240C=
ENST00000684288.1:c.*2294C= ENSP00000507143.1:n.*2294C=
ENST00000684313.1:n.3769C=
ENST00000684332.1:n.4410C=
ENST00000684371.1:n.4443C=
ENST00000684404.1:n.5365C=
ENST00000684442.1:n.4561C=
ENST00000684555.1:c.*2334C= ENSP00000507705.1:n.*2334C=
ENST00000684571.1:c.3963C= ENSP00000506935.1:p.Ile1321=
ENST00000684593.1:c.*3827C= ENSP00000507005.1:n.*3827C=
ENST00000684711.1:c.*2518C= ENSP00000506841.1:n.*2518C=
ENST00000302539.9:c.4125C= ENSP00000303960.4:p.Ile1375=
ENST00000389817.8:c.4122C= MANE Select ENSP00000374467.4:p.Ile1374=
ENST00000642271.1:c.4119C= ENSP00000493749.1:p.Ile1373=
ENST00000642579.1:c.2176C=
ENST00000642611.1:n.5207C=
ENST00000642902.1:c.3904C=
ENST00000643260.1:c.4122C= ENSP00000494450.1:p.Ile1374=
ENST00000643562.1:c.*2244C= ENSP00000496124.1:n.*2244C=
ENST00000643925.1:c.2762C=
ENST00000644057.1:n.199C=
ENST00000644484.1:c.*3508C= ENSP00000493558.1:n.*3508C=
ENST00000644675.1:c.*2294C= ENSP00000494567.1:n.*2294C=
ENST00000644757.1:c.*3202+336C= ENSP00000495085.1:n.*3202+336C=
ENST00000644772.1:c.4188C= ENSP00000494321.1:p.Ile1396=
ENST00000645004.1:n.1815C=
ENST00000645076.1:c.3321C=
ENST00000645417.1:c.1310C=
ENST00000645744.1:c.*3887C= ENSP00000494564.1:n.*3887C=
ENST00000645760.1:c.4543C=
ENST00000645884.1:c.*1405C= ENSP00000495516.1:n.*1405C=
ENST00000646003.1:c.*2224C= ENSP00000495259.1:n.*2224C=
ENST00000646207.1:c.*2959C= ENSP00000495025.1:n.*2959C=
ENST00000646276.1:c.*3526C= ENSP00000496070.1:n.*3526C=
ENST00000646592.1:c.3428C=
ENST00000646902.1:c.4089C= ENSP00000494101.1:p.Ile1363=
ENST00000646993.1:c.*2664C= ENSP00000493720.1:n.*2664C=
ENST00000647013.1:c.4128C= ENSP00000496741.1:n.4128C=
ENST00000647015.1:c.3873C= ENSP00000495389.1:p.Ile1291=
ENST00000647086.1:c.*3708C= ENSP00000493677.1:n.*3708C=
ENST00000647158.1:c.*2409C= ENSP00000495744.1:n.*2409C=
ENST00000302539.8:c.4125C= ENSP00000303960.4:p.Ile1375=
ENST00000389817.7:c.4122C= ENSP00000374467.3:p.Ile1374=
ENST00000528374.1:c.604C=
ENST00000532220.1:n.596C=
NM_000352.4:c.4122C= NP_000343.2:p.Ile1374=
NM_001287174.1:c.4125C= NP_001274103.1:p.Ile1375=
XM_011520331.1:c.4122C= XP_011518633.1:p.Ile1374=
XM_011520332.1:c.4125C= XP_011518634.1:p.Ile1375=
XM_011520333.1:c.2622C= XP_011518635.1:p.Ile874=
XR_930890.1:n.4188C=
NM_001351295.1:c.4188C= NP_001338224.1:p.Ile1396=
NM_001351296.1:c.4122C= NP_001338225.1:p.Ile1374=
NM_001351297.1:c.4119C= NP_001338226.1:p.Ile1373=
NR_147094.1:n.4417C=
XM_017018197.2:c.4191C= XP_016873686.1:p.Ile1397=
XM_017018199.1:c.4188C= XP_016873688.1:p.Ile1396=
XM_017018201.2:c.4191C= XP_016873690.1:p.Ile1397=
XM_017018202.1:c.2688C= XP_016873691.1:p.Ile896=
XM_017018204.1:c.2079C= XP_016873693.1:p.Ile693=
XM_024448668.1:c.2490C= XP_024304436.1:p.Ile830=
XR_001747945.2:n.4263C=
XR_001747946.2:n.4194C=
XR_002957189.1:n.5844C=
NM_000352.6:c.4122C= MANE Select NP_000343.2:p.Ile1374=
NM_001287174.2:c.4125C= NP_001274103.1:p.Ile1375=
NM_001351295.2:c.4188C= NP_001338224.1:p.Ile1396=
NM_001351296.2:c.4122C= NP_001338225.1:p.Ile1374=
NM_001351297.2:c.4119C= NP_001338226.1:p.Ile1373=
NR_147094.2:n.4417C=
NM_001287174.3:c.4125C= NP_001274103.1:p.Ile1375=