Canonical Allele Identifier: CA1955123895
Gene: ABCC8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17396921G= , CM000673.2:g.17396921G= GRCh38
NC_000011.9:g.17418468G= , CM000673.1:g.17418468G= GRCh37
NC_000011.8:g.17375044G= NCBI36
NG_008867.1:g.84982C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000524561.2:n.3715C=
ENST00000528374.2:c.705C=
ENST00000529967.6:n.2453C=
ENST00000532220.2:n.2362C=
ENST00000642611.2:n.4329C=
ENST00000644057.2:n.557C=
ENST00000645004.2:n.1613C=
ENST00000682051.1:n.4276C=
ENST00000682110.1:n.4329C=
ENST00000682140.1:c.3985+272C= ENSP00000507829.1:n.3985+272C=
ENST00000682185.1:n.5419C=
ENST00000682204.1:c.*2252C= ENSP00000507094.1:n.*2252C=
ENST00000682215.1:n.4696C=
ENST00000682288.1:c.*2545C= ENSP00000507506.1:n.*2545C=
ENST00000682442.1:n.4549C=
ENST00000682528.1:n.4406C=
ENST00000682673.1:n.4273C=
ENST00000682805.1:n.4696C=
ENST00000682965.1:c.*536C= ENSP00000508229.1:n.*536C=
ENST00000683093.1:n.4428C=
ENST00000683136.1:c.3997C= ENSP00000507768.1:p.Gln1333=
ENST00000683153.1:n.4371C=
ENST00000683365.1:n.4431C=
ENST00000683377.1:n.4329C=
ENST00000683456.1:c.*1251C= ENSP00000508318.1:n.*1251C=
ENST00000683522.1:n.4329C=
ENST00000683562.1:c.*2283C= ENSP00000508265.1:n.*2283C=
ENST00000683693.1:n.4776C=
ENST00000683725.1:c.4114C= ENSP00000507496.1:p.Gln1372=
ENST00000684010.1:n.4324C=
ENST00000684157.1:n.4329C=
ENST00000684253.1:n.4232C=
ENST00000684288.1:c.*2286C= ENSP00000507143.1:n.*2286C=
ENST00000684313.1:n.3761C=
ENST00000684332.1:n.4402C=
ENST00000684371.1:n.4435C=
ENST00000684404.1:n.4372C=
ENST00000684442.1:n.4553C=
ENST00000684555.1:c.*2326C= ENSP00000507705.1:n.*2326C=
ENST00000684571.1:c.3955C= ENSP00000506935.1:p.Gln1319=
ENST00000684593.1:c.*3819C= ENSP00000507005.1:n.*3819C=
ENST00000684711.1:c.*2510C= ENSP00000506841.1:n.*2510C=
ENST00000302539.9:c.4117C= ENSP00000303960.4:p.Gln1373=
ENST00000389817.8:c.4114C= MANE Select ENSP00000374467.4:p.Gln1372=
ENST00000642271.1:c.4111C= ENSP00000493749.1:p.Gln1371=
ENST00000642579.1:c.2168C=
ENST00000642611.1:n.4214C=
ENST00000642902.1:c.3896C=
ENST00000643260.1:c.4114C= ENSP00000494450.1:p.Gln1372=
ENST00000643562.1:c.*2236C= ENSP00000496124.1:n.*2236C=
ENST00000643925.1:c.2754C=
ENST00000644057.1:n.191C=
ENST00000644484.1:c.*2515C= ENSP00000493558.1:n.*2515C=
ENST00000644675.1:c.*2286C= ENSP00000494567.1:n.*2286C=
ENST00000644757.1:c.*2545C= ENSP00000495085.1:n.*2545C=
ENST00000644772.1:c.4180C= ENSP00000494321.1:p.Gln1394=
ENST00000645004.1:n.1769C=
ENST00000645076.1:c.3313C=
ENST00000645417.1:c.1302C=
ENST00000645744.1:c.*2894C= ENSP00000494564.1:n.*2894C=
ENST00000645760.1:c.4535C=
ENST00000645884.1:c.*1397C= ENSP00000495516.1:n.*1397C=
ENST00000646003.1:c.*2216C= ENSP00000495259.1:n.*2216C=
ENST00000646207.1:c.*2951C= ENSP00000495025.1:n.*2951C=
ENST00000646276.1:c.*2533C= ENSP00000496070.1:n.*2533C=
ENST00000646592.1:c.3420C=
ENST00000646902.1:c.4081C= ENSP00000494101.1:p.Gln1361=
ENST00000646993.1:c.*2656C= ENSP00000493720.1:n.*2656C=
ENST00000647013.1:c.4120C= ENSP00000496741.1:n.4120C=
ENST00000647015.1:c.3865C= ENSP00000495389.1:p.Gln1289=
ENST00000647086.1:c.*3700C= ENSP00000493677.1:n.*3700C=
ENST00000647158.1:c.*2401C= ENSP00000495744.1:n.*2401C=
ENST00000302539.8:c.4117C= ENSP00000303960.4:p.Gln1373=
ENST00000389817.7:c.4114C= ENSP00000374467.3:p.Gln1372=
ENST00000527905.5:c.*1136C= ENSP00000431653.1:n.*1136C=
ENST00000528374.1:c.596C=
ENST00000532220.1:n.588C=
NM_000352.4:c.4114C= NP_000343.2:p.Gln1372=
NM_001287174.1:c.4117C= NP_001274103.1:p.Gln1373=
XM_011520331.1:c.4114C= XP_011518633.1:p.Gln1372=
XM_011520332.1:c.4117C= XP_011518634.1:p.Gln1373=
XM_011520333.1:c.2614C= XP_011518635.1:p.Gln872=
XR_930890.1:n.4180C=
NM_001351295.1:c.4180C= NP_001338224.1:p.Gln1394=
NM_001351296.1:c.4114C= NP_001338225.1:p.Gln1372=
NM_001351297.1:c.4111C= NP_001338226.1:p.Gln1371=
NR_147094.1:n.4409C=
XM_017018197.2:c.4183C= XP_016873686.1:p.Gln1395=
XM_017018199.1:c.4180C= XP_016873688.1:p.Gln1394=
XM_017018201.2:c.4183C= XP_016873690.1:p.Gln1395=
XM_017018202.1:c.2680C= XP_016873691.1:p.Gln894=
XM_017018204.1:c.2071C= XP_016873693.1:p.Gln691=
XM_024448668.1:c.2482C= XP_024304436.1:p.Gln828=
XR_001747945.2:n.4255C=
XR_001747946.2:n.4186C=
XR_002957189.1:n.4851C=
NM_000352.6:c.4114C= MANE Select NP_000343.2:p.Gln1372=
NM_001287174.2:c.4117C= NP_001274103.1:p.Gln1373=
NM_001351295.2:c.4180C= NP_001338224.1:p.Gln1394=
NM_001351296.2:c.4114C= NP_001338225.1:p.Gln1372=
NM_001351297.2:c.4111C= NP_001338226.1:p.Gln1371=
NR_147094.2:n.4409C=
NM_001287174.3:c.4117C= NP_001274103.1:p.Gln1373=