Canonical Allele Identifier: CA1955138586
Gene: ABCC8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17428655G= , CM000673.2:g.17428655G= GRCh38
NC_000011.9:g.17450202G= , CM000673.1:g.17450202G= GRCh37
NC_000011.8:g.17406778G= NCBI36
NG_008867.1:g.53248C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000524561.2:n.1502C=
ENST00000642611.2:n.1899C=
ENST00000682051.1:n.1846C=
ENST00000682110.1:n.1899C=
ENST00000682140.1:c.1830C= ENSP00000507829.1:p.Ser610=
ENST00000682185.1:n.3138C=
ENST00000682204.1:c.1684C= ENSP00000507094.1:p.Arg562=
ENST00000682215.1:n.1899C=
ENST00000682288.1:c.*261C= ENSP00000507506.1:n.*261C=
ENST00000682442.1:n.2020C=
ENST00000682528.1:n.1899C=
ENST00000682673.1:n.1846C=
ENST00000682805.1:n.1899C=
ENST00000682965.1:c.1830C= ENSP00000508229.1:p.Ser610=
ENST00000683093.1:n.2001C=
ENST00000683136.1:c.1830C= ENSP00000507768.1:p.Ser610=
ENST00000683153.1:n.1899C=
ENST00000683253.1:n.2915C=
ENST00000683365.1:n.2001C=
ENST00000683377.1:n.1899C=
ENST00000683456.1:c.1830C= ENSP00000508318.1:p.Ser610=
ENST00000683522.1:n.1899C=
ENST00000683562.1:c.*2C= ENSP00000508265.1:n.*2C=
ENST00000683693.1:n.1899C=
ENST00000683725.1:c.1833C= ENSP00000507496.1:p.Ser611=
ENST00000684010.1:n.1899C=
ENST00000684157.1:n.1899C=
ENST00000684253.1:n.1805C=
ENST00000684288.1:c.*2C= ENSP00000507143.1:n.*2C=
ENST00000684313.1:n.1724-11693C=
ENST00000684332.1:n.1972C=
ENST00000684371.1:n.1846C=
ENST00000684404.1:n.1899C=
ENST00000684442.1:n.1899C=
ENST00000684555.1:c.*42C= ENSP00000507705.1:n.*42C=
ENST00000684571.1:c.1674C= ENSP00000506935.1:p.Ser558=
ENST00000684593.1:c.*1538C= ENSP00000507005.1:n.*1538C=
ENST00000684711.1:c.*229C= ENSP00000506841.1:n.*229C=
ENST00000302539.9:c.1833C= ENSP00000303960.4:p.Ser611=
ENST00000389817.8:c.1833C= MANE Select ENSP00000374467.4:p.Ser611=
ENST00000532728.6:c.1414C=
ENST00000642271.1:c.1830C= ENSP00000493749.1:p.Ser610=
ENST00000642611.1:n.1784C=
ENST00000642902.1:c.1668C=
ENST00000643260.1:c.1830C= ENSP00000494450.1:p.Ser610=
ENST00000643562.1:c.1833C= ENSP00000496124.1:p.Ser611=
ENST00000644447.1:c.186C= ENSP00000496282.1:p.Ser62=
ENST00000644472.1:c.*194C= ENSP00000495378.1:n.*194C=
ENST00000644484.1:c.*42C= ENSP00000493558.1:n.*42C=
ENST00000644542.1:c.*1535C= ENSP00000495532.1:n.*1535C=
ENST00000644649.1:c.1003C=
ENST00000644675.1:c.*2C= ENSP00000494567.1:n.*2C=
ENST00000644757.1:c.*135C= ENSP00000495085.1:n.*135C=
ENST00000644772.1:c.1833C= ENSP00000494321.1:p.Ser611=
ENST00000645076.1:c.1100-15C=
ENST00000645744.1:c.*194C= ENSP00000494564.1:n.*194C=
ENST00000645760.1:c.2108C=
ENST00000645884.1:c.1830C= ENSP00000495516.1:p.Ser610=
ENST00000646003.1:c.1684C= ENSP00000495259.1:p.Arg562=
ENST00000646207.1:c.*194C= ENSP00000495025.1:n.*194C=
ENST00000646276.1:c.*103C= ENSP00000496070.1:n.*103C=
ENST00000646592.1:c.897C=
ENST00000646902.1:c.1830C= ENSP00000494101.1:p.Ser610=
ENST00000646993.1:c.*229C= ENSP00000493720.1:n.*229C=
ENST00000647013.1:c.1836C= ENSP00000496741.1:n.1836C=
ENST00000647015.1:c.1672-250C= ENSP00000495389.1:n.1672-250C=
ENST00000647086.1:c.*1560C= ENSP00000493677.1:n.*1560C=
ENST00000647158.1:c.1684C= ENSP00000495744.1:p.Arg562=
ENST00000302539.8:c.1833C= ENSP00000303960.4:p.Ser611=
ENST00000389817.7:c.1833C= ENSP00000374467.3:p.Ser611=
ENST00000527905.5:c.1818-15C= ENSP00000431653.1:n.1818-15C=
NM_000352.4:c.1833C= NP_000343.2:p.Ser611=
NM_001287174.1:c.1833C= NP_001274103.1:p.Ser611=
XM_011520331.1:c.1830C= XP_011518633.1:p.Ser610=
XM_011520332.1:c.1833C= XP_011518634.1:p.Ser611=
XM_011520333.1:c.330C= XP_011518635.1:p.Ser110=
XM_011520334.1:c.1833C= XP_011518636.1:p.Ser611=
XR_930890.1:n.1896C=
XR_930891.1:n.1896C=
XR_930892.1:n.1896C=
XR_930893.1:n.1896C=
NM_001351295.1:c.1833C= NP_001338224.1:p.Ser611=
NM_001351296.1:c.1830C= NP_001338225.1:p.Ser610=
NM_001351297.1:c.1830C= NP_001338226.1:p.Ser610=
NR_147094.1:n.1899C=
XM_017018197.2:c.1833C= XP_016873686.1:p.Ser611=
XM_017018199.1:c.1830C= XP_016873688.1:p.Ser610=
XM_017018201.2:c.1833C= XP_016873690.1:p.Ser611=
XM_017018202.1:c.330C= XP_016873691.1:p.Ser110=
XM_017018204.1:c.-211C= XP_016873693.1:n.-211C=
XM_024448668.1:c.198C= XP_024304436.1:p.Ser66=
XR_001747945.2:n.1905C=
XR_001747946.2:n.1905C=
XR_002957189.1:n.1905C=
NM_000352.6:c.1833C= MANE Select NP_000343.2:p.Ser611=
NM_001287174.2:c.1833C= NP_001274103.1:p.Ser611=
NM_001351295.2:c.1833C= NP_001338224.1:p.Ser611=
NM_001351296.2:c.1830C= NP_001338225.1:p.Ser610=
NM_001351297.2:c.1830C= NP_001338226.1:p.Ser610=
NR_147094.2:n.1899C=
NM_001287174.3:c.1833C= NP_001274103.1:p.Ser611=