Canonical Allele Identifier: CA1955122306
Gene: ABCC8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17393736C= , CM000673.2:g.17393736C= GRCh38
NC_000011.9:g.17415283C= , CM000673.1:g.17415283C= GRCh37
NC_000011.8:g.17371859C= NCBI36
NG_008867.1:g.88167G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000524561.2:n.4170G=
ENST00000526037.6:n.504G=
ENST00000528374.2:c.1160G=
ENST00000529967.6:n.2908G=
ENST00000532220.2:n.3802G=
ENST00000642611.2:n.5902G=
ENST00000644057.2:n.1145G=
ENST00000645004.2:n.2068G=
ENST00000682051.1:n.4731G=
ENST00000682110.1:n.4784G=
ENST00000682140.1:c.*355G= ENSP00000507829.1:n.*355G=
ENST00000682185.1:n.5874G=
ENST00000682204.1:c.*2707G= ENSP00000507094.1:n.*2707G=
ENST00000682215.1:n.5151G=
ENST00000682288.1:c.*3000G= ENSP00000507506.1:n.*3000G=
ENST00000682442.1:n.5004G=
ENST00000682528.1:n.4861G=
ENST00000682673.1:n.4728G=
ENST00000682805.1:n.5189G=
ENST00000682965.1:c.*991G= ENSP00000508229.1:n.*991G=
ENST00000683093.1:n.5764G=
ENST00000683136.1:c.4452G= ENSP00000507768.1:p.Val1484=
ENST00000683153.1:n.4826G=
ENST00000683365.1:n.4886G=
ENST00000683377.1:n.4680G=
ENST00000683456.1:c.*1706G= ENSP00000508318.1:n.*1706G=
ENST00000683522.1:n.4866G=
ENST00000683562.1:c.*2634G= ENSP00000508265.1:n.*2634G=
ENST00000683693.1:n.6245G=
ENST00000683725.1:c.*34G= ENSP00000507496.1:n.*34G=
ENST00000684010.1:n.4779G=
ENST00000684014.1:n.756G=
ENST00000684157.1:n.5769G=
ENST00000684253.1:n.4687G=
ENST00000684288.1:c.*2741G= ENSP00000507143.1:n.*2741G=
ENST00000684313.1:n.4216G=
ENST00000684332.1:n.4857G=
ENST00000684371.1:n.4890G=
ENST00000684404.1:n.5812G=
ENST00000684442.1:n.5008G=
ENST00000684555.1:c.*2781G= ENSP00000507705.1:n.*2781G=
ENST00000684571.1:c.4410G= ENSP00000506935.1:p.Val1470=
ENST00000684593.1:c.*4274G= ENSP00000507005.1:n.*4274G=
ENST00000684711.1:c.*2965G= ENSP00000506841.1:n.*2965G=
ENST00000302539.9:c.4572G= ENSP00000303960.4:p.Val1524=
ENST00000389817.8:c.4569G= MANE Select ENSP00000374467.4:p.Val1523=
ENST00000642271.1:c.4566G= ENSP00000493749.1:p.Val1522=
ENST00000642579.1:c.2623G=
ENST00000642611.1:n.5787G=
ENST00000642902.1:c.4351G=
ENST00000643260.1:c.4569G= ENSP00000494450.1:p.Val1523=
ENST00000643562.1:c.*2691G= ENSP00000496124.1:n.*2691G=
ENST00000643925.1:c.3185+530G=
ENST00000644057.1:n.728G=
ENST00000644484.1:c.*3955G= ENSP00000493558.1:n.*3955G=
ENST00000644675.1:c.*2741G= ENSP00000494567.1:n.*2741G=
ENST00000644757.1:c.*3203-756G= ENSP00000495085.1:n.*3203-756G=
ENST00000644772.1:c.4635G= ENSP00000494321.1:p.Val1545=
ENST00000645004.1:n.2262G=
ENST00000645076.1:c.3664G=
ENST00000645417.1:c.1757G=
ENST00000645744.1:c.*4254G= ENSP00000494564.1:n.*4254G=
ENST00000645760.1:c.4990G=
ENST00000645884.1:c.*1852G= ENSP00000495516.1:n.*1852G=
ENST00000646003.1:c.*2591G= ENSP00000495259.1:n.*2591G=
ENST00000646207.1:c.*3406G= ENSP00000495025.1:n.*3406G=
ENST00000646276.1:c.*3973G= ENSP00000496070.1:n.*3973G=
ENST00000646592.1:c.3875G=
ENST00000646902.1:c.4536G= ENSP00000494101.1:p.Val1512=
ENST00000646993.1:c.*3007G= ENSP00000493720.1:n.*3007G=
ENST00000647015.1:c.4320G= ENSP00000495389.1:p.Val1440=
ENST00000647086.1:c.*4155G= ENSP00000493677.1:n.*4155G=
ENST00000647158.1:c.*2856G= ENSP00000495744.1:n.*2856G=
ENST00000302539.8:c.4572G= ENSP00000303960.4:p.Val1524=
ENST00000389817.7:c.4569G= ENSP00000374467.3:p.Val1523=
ENST00000525022.1:n.464G=
ENST00000526037.5:n.329G=
ENST00000526168.5:c.357G=
ENST00000531642.5:c.600G=
NM_000352.4:c.4569G= NP_000343.2:p.Val1523=
NM_001287174.1:c.4572G= NP_001274103.1:p.Val1524=
XM_011520331.1:c.4569G= XP_011518633.1:p.Val1523=
XM_011520333.1:c.3069G= XP_011518635.1:p.Val1023=
XR_930890.1:n.4531G=
NM_001351295.1:c.4635G= NP_001338224.1:p.Val1545=
NM_001351296.1:c.4569G= NP_001338225.1:p.Val1523=
NM_001351297.1:c.4566G= NP_001338226.1:p.Val1522=
NR_147094.1:n.4864G=
XM_017018197.2:c.4638G= XP_016873686.1:p.Val1546=
XM_017018199.1:c.4635G= XP_016873688.1:p.Val1545=
XM_017018202.1:c.3135G= XP_016873691.1:p.Val1045=
XM_017018204.1:c.2526G= XP_016873693.1:p.Val842=
XM_024448668.1:c.2937G= XP_024304436.1:p.Val979=
XR_001747945.2:n.4606G=
XR_001747946.2:n.4537G=
XR_002957189.1:n.6320G=
NM_000352.6:c.4569G= MANE Select NP_000343.2:p.Val1523=
NM_001287174.2:c.4572G= NP_001274103.1:p.Val1524=
NM_001351295.2:c.4635G= NP_001338224.1:p.Val1545=
NM_001351296.2:c.4569G= NP_001338225.1:p.Val1523=
NM_001351297.2:c.4566G= NP_001338226.1:p.Val1522=
NR_147094.2:n.4864G=
NM_001287174.3:c.4572G= NP_001274103.1:p.Val1524=