Canonical Allele Identifier: CA473303010
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 446765
dbSNP Id: rs1260178539

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17432244del , CM000673.2:g.17432244del GRCh38
NC_000011.9:g.17453791del , CM000673.1:g.17453791del GRCh37
NC_000011.8:g.17410367del NCBI36
NG_008867.1:g.49662del

Transcript Alleles

HGVS Amino-acid Change
ENST00000524561.2:n.1271del
ENST00000526002.2:n.1661del
ENST00000528202.6:n.1700del
ENST00000642611.2:n.1700del
ENST00000682051.1:n.1647del
ENST00000682110.1:n.1700del
ENST00000682140.1:c.1631del ENSP00000507829.1:p.Phe544SerfsTer2
ENST00000682185.1:n.2939del
ENST00000682199.1:n.1700del
ENST00000682204.1:c.1631del ENSP00000507094.1:p.Phe544SerfsTer2
ENST00000682215.1:n.1700del
ENST00000682288.1:c.1631del ENSP00000507506.1:p.Phe544SerfsTer2
ENST00000682442.1:n.1748del
ENST00000682528.1:n.1700del
ENST00000682673.1:n.1647del
ENST00000682805.1:n.1700del
ENST00000682965.1:c.1631del ENSP00000508229.1:p.Phe544SerfsTer2
ENST00000683093.1:n.1802del
ENST00000683136.1:c.1631del ENSP00000507768.1:p.Phe544SerfsTer2
ENST00000683153.1:n.1700del
ENST00000683253.1:n.2716del
ENST00000683365.1:n.1802del
ENST00000683377.1:n.1700del
ENST00000683456.1:c.1631del ENSP00000508318.1:p.Phe544SerfsTer2
ENST00000683522.1:n.1700del
ENST00000683531.1:n.1703del
ENST00000683562.1:c.1634del ENSP00000508265.1:p.Phe545SerfsTer2
ENST00000683693.1:n.1700del
ENST00000683725.1:c.1634del ENSP00000507496.1:p.Phe545SerfsTer2
ENST00000684010.1:n.1700del
ENST00000684157.1:n.1700del
ENST00000684253.1:n.1752del
ENST00000684288.1:c.1634del ENSP00000507143.1:p.Phe545SerfsTer2
ENST00000684313.1:n.1723+10479del
ENST00000684332.1:n.1700del
ENST00000684371.1:n.1647del
ENST00000684404.1:n.1700del
ENST00000684442.1:n.1700del
ENST00000684555.1:c.1634del ENSP00000507705.1:p.Phe545SerfsTer2
ENST00000684571.1:c.1475del ENSP00000506935.1:p.Phe492SerfsTer2
ENST00000684593.1:c.*1339del ENSP00000507005.1:n.*1339del
ENST00000684711.1:c.1631del ENSP00000506841.1:p.Phe544SerfsTer2
ENST00000302539.9:c.1634del ENSP00000303960.4:p.Phe545SerfsTer2
ENST00000389817.8:c.1634del MANE Select ENSP00000374467.4:p.Phe545SerfsTer2
ENST00000532728.6:c.1361del
ENST00000635881.1:n.1662del
ENST00000642271.1:c.1631del ENSP00000493749.1:p.Phe544SerfsTer2
ENST00000642611.1:n.1585del
ENST00000642902.1:c.1615del
ENST00000643260.1:c.1631del ENSP00000494450.1:p.Phe544SerfsTer2
ENST00000643562.1:c.1634del ENSP00000496124.1:p.Phe545SerfsTer2
ENST00000644472.1:c.1333del ENSP00000495378.1:p.Ser445HisfsTer?
ENST00000644484.1:c.1631del ENSP00000493558.1:p.Phe544SerfsTer2
ENST00000644542.1:c.*1336del ENSP00000495532.1:n.*1336del
ENST00000644649.1:c.804del
ENST00000644675.1:c.1631del ENSP00000494567.1:p.Phe544SerfsTer2
ENST00000644757.1:c.*50del ENSP00000495085.1:n.*50del
ENST00000644772.1:c.1634del ENSP00000494321.1:p.Phe545SerfsTer2
ENST00000645076.1:c.916del
ENST00000645744.1:c.1012del ENSP00000494564.1:p.Ser338HisfsTer?
ENST00000645760.1:c.1909del
ENST00000645884.1:c.1631del ENSP00000495516.1:p.Phe544SerfsTer2
ENST00000646003.1:c.1631del ENSP00000495259.1:p.Phe544SerfsTer2
ENST00000646207.1:c.1468del ENSP00000495025.1:p.Ser490HisfsTer?
ENST00000646276.1:c.*50del ENSP00000496070.1:n.*50del
ENST00000646592.1:c.882-3571del
ENST00000646902.1:c.1631del ENSP00000494101.1:p.Phe544SerfsTer2
ENST00000646993.1:c.1634del ENSP00000493720.1:p.Phe545SerfsTer2
ENST00000647013.1:c.1532del ENSP00000496741.1:p.Phe511SerfsTer2
ENST00000647015.1:c.1634del ENSP00000495389.1:p.Phe545SerfsTer2
ENST00000647086.1:c.1631del ENSP00000493677.1:p.Phe544SerfsTer2
ENST00000647158.1:c.1631del ENSP00000495744.1:p.Phe544SerfsTer2
ENST00000302539.8:c.1634del ENSP00000303960.4:p.Phe545SerfsTer2
ENST00000389817.7:c.1634del ENSP00000374467.3:p.Phe545SerfsTer2
ENST00000526002.1:n.423del
ENST00000527905.5:c.1634del ENSP00000431653.1:p.Phe545SerfsTer2
ENST00000528202.5:n.76del
ENST00000532728.5:n.1665del
NM_000352.4:c.1634del NP_000343.2:p.Phe545SerfsTer2
NM_001287174.1:c.1634del NP_001274103.1:p.Phe545SerfsTer2
XM_011520331.1:c.1631del XP_011518633.1:p.Phe544SerfsTer2
XM_011520332.1:c.1634del XP_011518634.1:p.Phe545SerfsTer2
XM_011520333.1:c.131del XP_011518635.1:p.Phe44SerfsTer2
XM_011520334.1:c.1634del XP_011518636.1:p.Phe545SerfsTer2
XR_930890.1:n.1697del
XR_930891.1:n.1697del
XR_930892.1:n.1697del
XR_930893.1:n.1697del
NM_001351295.1:c.1634del NP_001338224.1:p.Phe545SerfsTer2
NM_001351296.1:c.1631del NP_001338225.1:p.Phe544SerfsTer2
NM_001351297.1:c.1631del NP_001338226.1:p.Phe544SerfsTer2
NR_147094.1:n.1700del
XM_017018197.2:c.1634del XP_016873686.1:p.Phe545SerfsTer2
XM_017018199.1:c.1631del XP_016873688.1:p.Phe544SerfsTer2
XM_017018201.2:c.1634del XP_016873690.1:p.Phe545SerfsTer2
XM_017018202.1:c.131del XP_016873691.1:p.Phe44SerfsTer2
XM_017018204.1:c.-483del XP_016873693.1:n.-483del
XM_024448668.1:c.-2del XP_024304436.1:n.-2del
XR_001747945.2:n.1706del
XR_001747946.2:n.1706del
XR_002957189.1:n.1706del
NM_000352.6:c.1634del MANE Select NP_000343.2:p.Phe545SerfsTer2
NM_001287174.2:c.1634del NP_001274103.1:p.Phe545SerfsTer2
NM_001351295.2:c.1634del NP_001338224.1:p.Phe545SerfsTer2
NM_001351296.2:c.1631del NP_001338225.1:p.Phe544SerfsTer2
NM_001351297.2:c.1631del NP_001338226.1:p.Phe544SerfsTer2
NR_147094.2:n.1700del
NM_001287174.3:c.1634del NP_001274103.1:p.Phe545SerfsTer2