Canonical Allele Identifier: CA1955122950
Gene: ABCC8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17395145C= , CM000673.2:g.17395145C= GRCh38
NC_000011.9:g.17416692C= , CM000673.1:g.17416692C= GRCh37
NC_000011.8:g.17373268C= NCBI36
NG_008867.1:g.86758G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000524561.2:n.4012+27G=
ENST00000526037.6:n.346+27G=
ENST00000528374.2:c.1002+27G=
ENST00000529967.6:n.2750+27G=
ENST00000532220.2:n.3644+27G=
ENST00000642611.2:n.5744+27G=
ENST00000644057.2:n.987+27G=
ENST00000645004.2:n.1910+27G=
ENST00000682051.1:n.4573+27G=
ENST00000682110.1:n.4626+27G=
ENST00000682140.1:c.*197+27G= ENSP00000507829.1:n.*197+27G=
ENST00000682185.1:n.5716+27G=
ENST00000682204.1:c.*2549+27G= ENSP00000507094.1:n.*2549+27G=
ENST00000682215.1:n.4993+27G=
ENST00000682288.1:c.*2842+27G= ENSP00000507506.1:n.*2842+27G=
ENST00000682442.1:n.4846+27G=
ENST00000682528.1:n.4703+27G=
ENST00000682673.1:n.4570+27G=
ENST00000682805.1:n.5031+27G=
ENST00000682965.1:c.*833+27G= ENSP00000508229.1:n.*833+27G=
ENST00000683093.1:n.5606+465G=
ENST00000683136.1:c.4294+27G= ENSP00000507768.1:n.4294+27G=
ENST00000683153.1:n.4668+27G=
ENST00000683365.1:n.4728+27G=
ENST00000683377.1:n.4522+465G=
ENST00000683456.1:c.*1548+27G= ENSP00000508318.1:n.*1548+27G=
ENST00000683522.1:n.4653G=
ENST00000683562.1:c.*2476+465G= ENSP00000508265.1:n.*2476+465G=
ENST00000683693.1:n.6087+465G=
ENST00000683725.1:c.4307+465G= ENSP00000507496.1:n.4307+465G=
ENST00000684010.1:n.4621+27G=
ENST00000684157.1:n.5611+27G=
ENST00000684253.1:n.4529+27G=
ENST00000684288.1:c.*2583+27G= ENSP00000507143.1:n.*2583+27G=
ENST00000684313.1:n.4058+27G=
ENST00000684332.1:n.4699+27G=
ENST00000684371.1:n.4732+27G=
ENST00000684404.1:n.5654+27G=
ENST00000684442.1:n.4850+27G=
ENST00000684555.1:c.*2623+27G= ENSP00000507705.1:n.*2623+27G=
ENST00000684571.1:c.4252+27G= ENSP00000506935.1:n.4252+27G=
ENST00000684593.1:c.*4116+27G= ENSP00000507005.1:n.*4116+27G=
ENST00000684711.1:c.*2807+27G= ENSP00000506841.1:n.*2807+27G=
ENST00000302539.9:c.4414+27G= ENSP00000303960.4:n.4414+27G=
ENST00000389817.8:c.4411+27G= MANE Select ENSP00000374467.4:n.4411+27G=
ENST00000642271.1:c.4408+27G= ENSP00000493749.1:n.4408+27G=
ENST00000642579.1:c.2465+27G=
ENST00000642611.1:n.5629+27G=
ENST00000642902.1:c.4193+27G=
ENST00000643260.1:c.4411+27G= ENSP00000494450.1:n.4411+27G=
ENST00000643562.1:c.*2533+27G= ENSP00000496124.1:n.*2533+27G=
ENST00000643925.1:c.3051+27G=
ENST00000644057.1:n.515G=
ENST00000644484.1:c.*3797+27G= ENSP00000493558.1:n.*3797+27G=
ENST00000644675.1:c.*2583+27G= ENSP00000494567.1:n.*2583+27G=
ENST00000644757.1:c.*3202+1119G= ENSP00000495085.1:n.*3202+1119G=
ENST00000644772.1:c.4477+27G= ENSP00000494321.1:n.4477+27G=
ENST00000645004.1:n.2104+27G=
ENST00000645076.1:c.3506+465G=
ENST00000645417.1:c.1599+27G=
ENST00000645744.1:c.*4096+27G= ENSP00000494564.1:n.*4096+27G=
ENST00000645760.1:c.4832+27G=
ENST00000645884.1:c.*1694+27G= ENSP00000495516.1:n.*1694+27G=
ENST00000646003.1:c.*2433+27G= ENSP00000495259.1:n.*2433+27G=
ENST00000646207.1:c.*3248+27G= ENSP00000495025.1:n.*3248+27G=
ENST00000646276.1:c.*3815+27G= ENSP00000496070.1:n.*3815+27G=
ENST00000646592.1:c.3717+27G=
ENST00000646902.1:c.4378+27G= ENSP00000494101.1:n.4378+27G=
ENST00000646993.1:c.*2849+465G= ENSP00000493720.1:n.*2849+465G=
ENST00000647013.1:c.4417+27G= ENSP00000496741.1:n.4417+27G=
ENST00000647015.1:c.4162+27G= ENSP00000495389.1:n.4162+27G=
ENST00000647086.1:c.*3997+27G= ENSP00000493677.1:n.*3997+27G=
ENST00000647158.1:c.*2698+27G= ENSP00000495744.1:n.*2698+27G=
ENST00000302539.8:c.4414+27G= ENSP00000303960.4:n.4414+27G=
ENST00000389817.7:c.4411+27G= ENSP00000374467.3:n.4411+27G=
ENST00000525022.1:n.306+465G=
ENST00000526037.5:n.171+465G=
ENST00000526168.5:c.199+27G=
ENST00000531642.5:c.442+27G=
NM_000352.4:c.4411+27G= NP_000343.2:n.4411+27G=
NM_001287174.1:c.4414+27G= NP_001274103.1:n.4414+27G=
XM_011520331.1:c.4411+27G= XP_011518633.1:n.4411+27G=
XM_011520332.1:c.4310+465G= XP_011518634.1:n.4310+465G=
XM_011520333.1:c.2911+27G= XP_011518635.1:n.2911+27G=
XR_930890.1:n.4373+465G=
NM_001351295.1:c.4477+27G= NP_001338224.1:n.4477+27G=
NM_001351296.1:c.4411+27G= NP_001338225.1:n.4411+27G=
NM_001351297.1:c.4408+27G= NP_001338226.1:n.4408+27G=
NR_147094.1:n.4706+27G=
XM_017018197.2:c.4480+27G= XP_016873686.1:n.4480+27G=
XM_017018199.1:c.4477+27G= XP_016873688.1:n.4477+27G=
XM_017018201.2:c.4376+465G= XP_016873690.1:n.4376+465G=
XM_017018202.1:c.2977+27G= XP_016873691.1:n.2977+27G=
XM_017018204.1:c.2368+27G= XP_016873693.1:n.2368+27G=
XM_024448668.1:c.2779+27G= XP_024304436.1:n.2779+27G=
XR_001747945.2:n.4448+465G=
XR_001747946.2:n.4379+465G=
XR_002957189.1:n.6162+465G=
NM_000352.6:c.4411+27G= MANE Select NP_000343.2:n.4411+27G=
NM_001287174.2:c.4414+27G= NP_001274103.1:n.4414+27G=
NM_001351295.2:c.4477+27G= NP_001338224.1:n.4477+27G=
NM_001351296.2:c.4411+27G= NP_001338225.1:n.4411+27G=
NM_001351297.2:c.4408+27G= NP_001338226.1:n.4408+27G=
NR_147094.2:n.4706+27G=
NM_001287174.3:c.4414+27G= NP_001274103.1:n.4414+27G=