Canonical Allele Identifier: CA379815448
Gene: ABCC8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17428399T>A , CM000673.2:g.17428399T>A GRCh38
NC_000011.9:g.17449946T>A , CM000673.1:g.17449946T>A GRCh37
NC_000011.8:g.17406522T>A NCBI36
NG_008867.1:g.53504A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000524561.2:n.1599A>T
ENST00000529967.6:n.189A>T
ENST00000642611.2:n.1996A>T
ENST00000682051.1:n.1943A>T
ENST00000682110.1:n.1996A>T
ENST00000682140.1:c.1927A>T ENSP00000507829.1:p.Arg643Trp
ENST00000682185.1:n.3235A>T
ENST00000682204.1:c.*68A>T ENSP00000507094.1:n.*68A>T
ENST00000682215.1:n.1996A>T
ENST00000682288.1:c.*358A>T ENSP00000507506.1:n.*358A>T
ENST00000682442.1:n.2117A>T
ENST00000682528.1:n.1996A>T
ENST00000682673.1:n.1943A>T
ENST00000682805.1:n.1996A>T
ENST00000682965.1:c.1927A>T ENSP00000508229.1:p.Arg643Trp
ENST00000683093.1:n.2098A>T
ENST00000683136.1:c.1927A>T ENSP00000507768.1:p.Arg643Trp
ENST00000683153.1:n.2155A>T
ENST00000683253.1:n.3012A>T
ENST00000683365.1:n.2098A>T
ENST00000683377.1:n.1996A>T
ENST00000683456.1:c.1927A>T ENSP00000508318.1:p.Arg643Trp
ENST00000683522.1:n.1996A>T
ENST00000683562.1:c.*99A>T ENSP00000508265.1:n.*99A>T
ENST00000683693.1:n.1996A>T
ENST00000683725.1:c.1930A>T ENSP00000507496.1:p.Arg644Trp
ENST00000684010.1:n.1996A>T
ENST00000684157.1:n.1996A>T
ENST00000684253.1:n.1902A>T
ENST00000684288.1:c.*99A>T ENSP00000507143.1:n.*99A>T
ENST00000684313.1:n.1724-11437A>T
ENST00000684332.1:n.2069A>T
ENST00000684371.1:n.2102A>T
ENST00000684404.1:n.1996A>T
ENST00000684442.1:n.1996A>T
ENST00000684555.1:c.*139A>T ENSP00000507705.1:n.*139A>T
ENST00000684571.1:c.1771A>T ENSP00000506935.1:p.Arg591Trp
ENST00000684593.1:c.*1635A>T ENSP00000507005.1:n.*1635A>T
ENST00000684711.1:c.*326A>T ENSP00000506841.1:n.*326A>T
ENST00000302539.9:c.1930A>T ENSP00000303960.4:p.Arg644Trp
ENST00000389817.8:c.1930A>T MANE Select ENSP00000374467.4:p.Arg644Trp
ENST00000532728.6:c.1511A>T
ENST00000642271.1:c.1927A>T ENSP00000493749.1:p.Arg643Trp
ENST00000642579.1:c.11A>T
ENST00000642611.1:n.1881A>T
ENST00000642902.1:c.1765A>T
ENST00000643260.1:c.1927A>T ENSP00000494450.1:p.Arg643Trp
ENST00000643562.1:c.1924-2A>T ENSP00000496124.1:n.1924-2A>T
ENST00000644447.1:c.283A>T ENSP00000496282.1:p.Arg95Trp
ENST00000644472.1:c.*291A>T ENSP00000495378.1:n.*291A>T
ENST00000644484.1:c.*139A>T ENSP00000493558.1:n.*139A>T
ENST00000644542.1:c.*1632A>T ENSP00000495532.1:n.*1632A>T
ENST00000644649.1:c.1100A>T
ENST00000644675.1:c.*99A>T ENSP00000494567.1:n.*99A>T
ENST00000644757.1:c.*232A>T ENSP00000495085.1:n.*232A>T
ENST00000644772.1:c.1996A>T ENSP00000494321.1:p.Arg666Trp
ENST00000645076.1:c.1182A>T
ENST00000645744.1:c.*291A>T ENSP00000494564.1:n.*291A>T
ENST00000645760.1:c.2205A>T
ENST00000645884.1:c.1927A>T ENSP00000495516.1:p.Arg643Trp
ENST00000646003.1:c.*68A>T ENSP00000495259.1:n.*68A>T
ENST00000646207.1:c.*291A>T ENSP00000495025.1:n.*291A>T
ENST00000646276.1:c.*200A>T ENSP00000496070.1:n.*200A>T
ENST00000646592.1:c.1153A>T
ENST00000646902.1:c.1927A>T ENSP00000494101.1:p.Arg643Trp
ENST00000646993.1:c.*326A>T ENSP00000493720.1:n.*326A>T
ENST00000647013.1:c.1933A>T ENSP00000496741.1:n.1933A>T
ENST00000647015.1:c.1678A>T ENSP00000495389.1:p.Arg560Trp
ENST00000647086.1:c.*1657A>T ENSP00000493677.1:n.*1657A>T
ENST00000647158.1:c.*68A>T ENSP00000495744.1:n.*68A>T
ENST00000302539.8:c.1930A>T ENSP00000303960.4:p.Arg644Trp
ENST00000389817.7:c.1930A>T ENSP00000374467.3:p.Arg644Trp
ENST00000527905.5:c.1900A>T ENSP00000431653.1:p.Arg634Trp
NM_000352.4:c.1930A>T NP_000343.2:p.Arg644Trp
NM_001287174.1:c.1930A>T NP_001274103.1:p.Arg644Trp
XM_011520331.1:c.1927A>T XP_011518633.1:p.Arg643Trp
XM_011520332.1:c.1930A>T XP_011518634.1:p.Arg644Trp
XM_011520333.1:c.427A>T XP_011518635.1:p.Arg143Trp
XM_011520334.1:c.1930A>T XP_011518636.1:p.Arg644Trp
XR_930890.1:n.1993A>T
XR_930891.1:n.1993A>T
XR_930892.1:n.1993A>T
XR_930893.1:n.1993A>T
NM_001351295.1:c.1996A>T NP_001338224.1:p.Arg666Trp
NM_001351296.1:c.1927A>T NP_001338225.1:p.Arg643Trp
NM_001351297.1:c.1927A>T NP_001338226.1:p.Arg643Trp
NR_147094.1:n.1996A>T
XM_017018197.2:c.1996A>T XP_016873686.1:p.Arg666Trp
XM_017018199.1:c.1993A>T XP_016873688.1:p.Arg665Trp
XM_017018201.2:c.1996A>T XP_016873690.1:p.Arg666Trp
XM_017018202.1:c.493A>T XP_016873691.1:p.Arg165Trp
XM_017018204.1:c.-114A>T XP_016873693.1:n.-114A>T
XM_024448668.1:c.295A>T XP_024304436.1:p.Arg99Trp
XR_001747945.2:n.2068A>T
XR_001747946.2:n.2002A>T
XR_002957189.1:n.2068A>T
NM_000352.6:c.1930A>T MANE Select NP_000343.2:p.Arg644Trp
NM_001287174.2:c.1930A>T NP_001274103.1:p.Arg644Trp
NM_001351295.2:c.1996A>T NP_001338224.1:p.Arg666Trp
NM_001351296.2:c.1927A>T NP_001338225.1:p.Arg643Trp
NM_001351297.2:c.1927A>T NP_001338226.1:p.Arg643Trp
NR_147094.2:n.1996A>T
NM_001287174.3:c.1930A>T NP_001274103.1:p.Arg644Trp