Canonical Allele Identifier: CA1955138583
Gene: ABCC8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17428650A= , CM000673.2:g.17428650A= GRCh38
NC_000011.9:g.17450197A= , CM000673.1:g.17450197A= GRCh37
NC_000011.8:g.17406773A= NCBI36
NG_008867.1:g.53253T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000524561.2:n.1507T=
ENST00000642611.2:n.1904T=
ENST00000682051.1:n.1851T=
ENST00000682110.1:n.1904T=
ENST00000682140.1:c.1835T= ENSP00000507829.1:p.Phe612=
ENST00000682185.1:n.3143T=
ENST00000682204.1:c.1689T= ENSP00000507094.1:p.Val563=
ENST00000682215.1:n.1904T=
ENST00000682288.1:c.*266T= ENSP00000507506.1:n.*266T=
ENST00000682442.1:n.2025T=
ENST00000682528.1:n.1904T=
ENST00000682673.1:n.1851T=
ENST00000682805.1:n.1904T=
ENST00000682965.1:c.1835T= ENSP00000508229.1:p.Phe612=
ENST00000683093.1:n.2006T=
ENST00000683136.1:c.1835T= ENSP00000507768.1:p.Phe612=
ENST00000683153.1:n.1904T=
ENST00000683253.1:n.2920T=
ENST00000683365.1:n.2006T=
ENST00000683377.1:n.1904T=
ENST00000683456.1:c.1835T= ENSP00000508318.1:p.Phe612=
ENST00000683522.1:n.1904T=
ENST00000683562.1:c.*7T= ENSP00000508265.1:n.*7T=
ENST00000683693.1:n.1904T=
ENST00000683725.1:c.1838T= ENSP00000507496.1:p.Phe613=
ENST00000684010.1:n.1904T=
ENST00000684157.1:n.1904T=
ENST00000684253.1:n.1810T=
ENST00000684288.1:c.*7T= ENSP00000507143.1:n.*7T=
ENST00000684313.1:n.1724-11688T=
ENST00000684332.1:n.1977T=
ENST00000684371.1:n.1851T=
ENST00000684404.1:n.1904T=
ENST00000684442.1:n.1904T=
ENST00000684555.1:c.*47T= ENSP00000507705.1:n.*47T=
ENST00000684571.1:c.1679T= ENSP00000506935.1:p.Phe560=
ENST00000684593.1:c.*1543T= ENSP00000507005.1:n.*1543T=
ENST00000684711.1:c.*234T= ENSP00000506841.1:n.*234T=
ENST00000302539.9:c.1838T= ENSP00000303960.4:p.Phe613=
ENST00000389817.8:c.1838T= MANE Select ENSP00000374467.4:p.Phe613=
ENST00000532728.6:c.1419T=
ENST00000642271.1:c.1835T= ENSP00000493749.1:p.Phe612=
ENST00000642611.1:n.1789T=
ENST00000642902.1:c.1673T=
ENST00000643260.1:c.1835T= ENSP00000494450.1:p.Phe612=
ENST00000643562.1:c.1838T= ENSP00000496124.1:p.Phe613=
ENST00000644447.1:c.191T= ENSP00000496282.1:p.Phe64=
ENST00000644472.1:c.*199T= ENSP00000495378.1:n.*199T=
ENST00000644484.1:c.*47T= ENSP00000493558.1:n.*47T=
ENST00000644542.1:c.*1540T= ENSP00000495532.1:n.*1540T=
ENST00000644649.1:c.1008T=
ENST00000644675.1:c.*7T= ENSP00000494567.1:n.*7T=
ENST00000644757.1:c.*140T= ENSP00000495085.1:n.*140T=
ENST00000644772.1:c.1838T= ENSP00000494321.1:p.Phe613=
ENST00000645076.1:c.1100-10T=
ENST00000645744.1:c.*199T= ENSP00000494564.1:n.*199T=
ENST00000645760.1:c.2113T=
ENST00000645884.1:c.1835T= ENSP00000495516.1:p.Phe612=
ENST00000646003.1:c.1689T= ENSP00000495259.1:p.Val563=
ENST00000646207.1:c.*199T= ENSP00000495025.1:n.*199T=
ENST00000646276.1:c.*108T= ENSP00000496070.1:n.*108T=
ENST00000646592.1:c.902T=
ENST00000646902.1:c.1835T= ENSP00000494101.1:p.Phe612=
ENST00000646993.1:c.*234T= ENSP00000493720.1:n.*234T=
ENST00000647013.1:c.1841T= ENSP00000496741.1:n.1841T=
ENST00000647015.1:c.1672-245T= ENSP00000495389.1:n.1672-245T=
ENST00000647086.1:c.*1565T= ENSP00000493677.1:n.*1565T=
ENST00000647158.1:c.1689T= ENSP00000495744.1:p.Val563=
ENST00000302539.8:c.1838T= ENSP00000303960.4:p.Phe613=
ENST00000389817.7:c.1838T= ENSP00000374467.3:p.Phe613=
ENST00000527905.5:c.1818-10T= ENSP00000431653.1:n.1818-10T=
NM_000352.4:c.1838T= NP_000343.2:p.Phe613=
NM_001287174.1:c.1838T= NP_001274103.1:p.Phe613=
XM_011520331.1:c.1835T= XP_011518633.1:p.Phe612=
XM_011520332.1:c.1838T= XP_011518634.1:p.Phe613=
XM_011520333.1:c.335T= XP_011518635.1:p.Phe112=
XM_011520334.1:c.1838T= XP_011518636.1:p.Phe613=
XR_930890.1:n.1901T=
XR_930891.1:n.1901T=
XR_930892.1:n.1901T=
XR_930893.1:n.1901T=
NM_001351295.1:c.1838T= NP_001338224.1:p.Phe613=
NM_001351296.1:c.1835T= NP_001338225.1:p.Phe612=
NM_001351297.1:c.1835T= NP_001338226.1:p.Phe612=
NR_147094.1:n.1904T=
XM_017018197.2:c.1838T= XP_016873686.1:p.Phe613=
XM_017018199.1:c.1835T= XP_016873688.1:p.Phe612=
XM_017018201.2:c.1838T= XP_016873690.1:p.Phe613=
XM_017018202.1:c.335T= XP_016873691.1:p.Phe112=
XM_017018204.1:c.-206T= XP_016873693.1:n.-206T=
XM_024448668.1:c.203T= XP_024304436.1:p.Phe68=
XR_001747945.2:n.1910T=
XR_001747946.2:n.1910T=
XR_002957189.1:n.1910T=
NM_000352.6:c.1838T= MANE Select NP_000343.2:p.Phe613=
NM_001287174.2:c.1838T= NP_001274103.1:p.Phe613=
NM_001351295.2:c.1838T= NP_001338224.1:p.Phe613=
NM_001351296.2:c.1835T= NP_001338225.1:p.Phe612=
NM_001351297.2:c.1835T= NP_001338226.1:p.Phe612=
NR_147094.2:n.1904T=
NM_001287174.3:c.1838T= NP_001274103.1:p.Phe613=