Canonical Allele Identifier: CA1955138448
Gene: ABCC8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17428396C= , CM000673.2:g.17428396C= GRCh38
NC_000011.9:g.17449943C= , CM000673.1:g.17449943C= GRCh37
NC_000011.8:g.17406519C= NCBI36
NG_008867.1:g.53507G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000524561.2:n.1602G=
ENST00000529967.6:n.192G=
ENST00000642611.2:n.1999G=
ENST00000682051.1:n.1946G=
ENST00000682110.1:n.1999G=
ENST00000682140.1:c.1930G= ENSP00000507829.1:p.Val644=
ENST00000682185.1:n.3238G=
ENST00000682204.1:c.*71G= ENSP00000507094.1:n.*71G=
ENST00000682215.1:n.1999G=
ENST00000682288.1:c.*361G= ENSP00000507506.1:n.*361G=
ENST00000682442.1:n.2120G=
ENST00000682528.1:n.1999G=
ENST00000682673.1:n.1946G=
ENST00000682805.1:n.1999G=
ENST00000682965.1:c.1930G= ENSP00000508229.1:p.Val644=
ENST00000683093.1:n.2101G=
ENST00000683136.1:c.1930G= ENSP00000507768.1:p.Val644=
ENST00000683153.1:n.2158G=
ENST00000683253.1:n.3015G=
ENST00000683365.1:n.2101G=
ENST00000683377.1:n.1999G=
ENST00000683456.1:c.1930G= ENSP00000508318.1:p.Val644=
ENST00000683522.1:n.1999G=
ENST00000683562.1:c.*102G= ENSP00000508265.1:n.*102G=
ENST00000683693.1:n.1999G=
ENST00000683725.1:c.1933G= ENSP00000507496.1:p.Val645=
ENST00000684010.1:n.1999G=
ENST00000684157.1:n.1999G=
ENST00000684253.1:n.1905G=
ENST00000684288.1:c.*102G= ENSP00000507143.1:n.*102G=
ENST00000684313.1:n.1724-11434G=
ENST00000684332.1:n.2072G=
ENST00000684371.1:n.2105G=
ENST00000684404.1:n.1999G=
ENST00000684442.1:n.1999G=
ENST00000684555.1:c.*142G= ENSP00000507705.1:n.*142G=
ENST00000684571.1:c.1774G= ENSP00000506935.1:p.Val592=
ENST00000684593.1:c.*1638G= ENSP00000507005.1:n.*1638G=
ENST00000684711.1:c.*329G= ENSP00000506841.1:n.*329G=
ENST00000302539.9:c.1933G= ENSP00000303960.4:p.Val645=
ENST00000389817.8:c.1933G= MANE Select ENSP00000374467.4:p.Val645=
ENST00000532728.6:c.1514G=
ENST00000642271.1:c.1930G= ENSP00000493749.1:p.Val644=
ENST00000642579.1:c.14G=
ENST00000642611.1:n.1884G=
ENST00000642902.1:c.1768G=
ENST00000643260.1:c.1930G= ENSP00000494450.1:p.Val644=
ENST00000643562.1:c.1925G= ENSP00000496124.1:p.Gly642=
ENST00000644447.1:c.286G= ENSP00000496282.1:p.Val96=
ENST00000644472.1:c.*294G= ENSP00000495378.1:n.*294G=
ENST00000644484.1:c.*142G= ENSP00000493558.1:n.*142G=
ENST00000644542.1:c.*1635G= ENSP00000495532.1:n.*1635G=
ENST00000644649.1:c.1103G=
ENST00000644675.1:c.*102G= ENSP00000494567.1:n.*102G=
ENST00000644757.1:c.*235G= ENSP00000495085.1:n.*235G=
ENST00000644772.1:c.1999G= ENSP00000494321.1:p.Val667=
ENST00000645076.1:c.1185G=
ENST00000645744.1:c.*294G= ENSP00000494564.1:n.*294G=
ENST00000645760.1:c.2208G=
ENST00000645884.1:c.1930G= ENSP00000495516.1:p.Val644=
ENST00000646003.1:c.*71G= ENSP00000495259.1:n.*71G=
ENST00000646207.1:c.*294G= ENSP00000495025.1:n.*294G=
ENST00000646276.1:c.*203G= ENSP00000496070.1:n.*203G=
ENST00000646592.1:c.1156G=
ENST00000646902.1:c.1930G= ENSP00000494101.1:p.Val644=
ENST00000646993.1:c.*329G= ENSP00000493720.1:n.*329G=
ENST00000647013.1:c.1936G= ENSP00000496741.1:n.1936G=
ENST00000647015.1:c.1681G= ENSP00000495389.1:p.Val561=
ENST00000647086.1:c.*1660G= ENSP00000493677.1:n.*1660G=
ENST00000647158.1:c.*71G= ENSP00000495744.1:n.*71G=
ENST00000302539.8:c.1933G= ENSP00000303960.4:p.Val645=
ENST00000389817.7:c.1933G= ENSP00000374467.3:p.Val645=
ENST00000527905.5:c.1903G= ENSP00000431653.1:p.Val635=
NM_000352.4:c.1933G= NP_000343.2:p.Val645=
NM_001287174.1:c.1933G= NP_001274103.1:p.Val645=
XM_011520331.1:c.1930G= XP_011518633.1:p.Val644=
XM_011520332.1:c.1933G= XP_011518634.1:p.Val645=
XM_011520333.1:c.430G= XP_011518635.1:p.Val144=
XM_011520334.1:c.1933G= XP_011518636.1:p.Val645=
XR_930890.1:n.1996G=
XR_930891.1:n.1996G=
XR_930892.1:n.1996G=
XR_930893.1:n.1996G=
NM_001351295.1:c.1999G= NP_001338224.1:p.Val667=
NM_001351296.1:c.1930G= NP_001338225.1:p.Val644=
NM_001351297.1:c.1930G= NP_001338226.1:p.Val644=
NR_147094.1:n.1999G=
XM_017018197.2:c.1999G= XP_016873686.1:p.Val667=
XM_017018199.1:c.1996G= XP_016873688.1:p.Val666=
XM_017018201.2:c.1999G= XP_016873690.1:p.Val667=
XM_017018202.1:c.496G= XP_016873691.1:p.Val166=
XM_017018204.1:c.-111G= XP_016873693.1:n.-111G=
XM_024448668.1:c.298G= XP_024304436.1:p.Val100=
XR_001747945.2:n.2071G=
XR_001747946.2:n.2005G=
XR_002957189.1:n.2071G=
NM_000352.6:c.1933G= MANE Select NP_000343.2:p.Val645=
NM_001287174.2:c.1933G= NP_001274103.1:p.Val645=
NM_001351295.2:c.1999G= NP_001338224.1:p.Val667=
NM_001351296.2:c.1930G= NP_001338225.1:p.Val644=
NM_001351297.2:c.1930G= NP_001338226.1:p.Val644=
NR_147094.2:n.1999G=
NM_001287174.3:c.1933G= NP_001274103.1:p.Val645=