Canonical Allele Identifier: CA1955123273
Gene: ABCC8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17395725G= , CM000673.2:g.17395725G= GRCh38
NC_000011.9:g.17417272G= , CM000673.1:g.17417272G= GRCh37
NC_000011.8:g.17373848G= NCBI36
NG_008867.1:g.86178C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000524561.2:n.3800-7C=
ENST00000528374.2:c.790-7C=
ENST00000529967.6:n.2538-7C=
ENST00000532220.2:n.3432-7C=
ENST00000642611.2:n.5525C=
ENST00000644057.2:n.768C=
ENST00000645004.2:n.1698-7C=
ENST00000682051.1:n.4361-7C=
ENST00000682110.1:n.4414-7C=
ENST00000682140.1:c.4065-7C= ENSP00000507829.1:n.4065-7C=
ENST00000682185.1:n.5504-7C=
ENST00000682204.1:c.*2337-7C= ENSP00000507094.1:n.*2337-7C=
ENST00000682215.1:n.4781-7C=
ENST00000682288.1:c.*2630-7C= ENSP00000507506.1:n.*2630-7C=
ENST00000682442.1:n.4634-7C=
ENST00000682528.1:n.4491-7C=
ENST00000682673.1:n.4358-7C=
ENST00000682805.1:n.4819-7C=
ENST00000682965.1:c.*621-7C= ENSP00000508229.1:n.*621-7C=
ENST00000683093.1:n.5498-7C=
ENST00000683136.1:c.4082-7C= ENSP00000507768.1:n.4082-7C=
ENST00000683153.1:n.4456-7C=
ENST00000683365.1:n.4516-7C=
ENST00000683377.1:n.4414-7C=
ENST00000683456.1:c.*1336-7C= ENSP00000508318.1:n.*1336-7C=
ENST00000683522.1:n.4414-7C=
ENST00000683562.1:c.*2368-7C= ENSP00000508265.1:n.*2368-7C=
ENST00000683693.1:n.5972C=
ENST00000683725.1:c.4199-7C= ENSP00000507496.1:n.4199-7C=
ENST00000684010.1:n.4409-7C=
ENST00000684157.1:n.5399-7C=
ENST00000684253.1:n.4317-7C=
ENST00000684288.1:c.*2371-7C= ENSP00000507143.1:n.*2371-7C=
ENST00000684313.1:n.3846-7C=
ENST00000684332.1:n.4487-7C=
ENST00000684371.1:n.4520-7C=
ENST00000684404.1:n.5442-7C=
ENST00000684442.1:n.4638-7C=
ENST00000684555.1:c.*2411-7C= ENSP00000507705.1:n.*2411-7C=
ENST00000684571.1:c.4040-7C= ENSP00000506935.1:n.4040-7C=
ENST00000684593.1:c.*3904-7C= ENSP00000507005.1:n.*3904-7C=
ENST00000684711.1:c.*2595-7C= ENSP00000506841.1:n.*2595-7C=
ENST00000302539.9:c.4202-7C= ENSP00000303960.4:n.4202-7C=
ENST00000389817.8:c.4199-7C= MANE Select ENSP00000374467.4:n.4199-7C=
ENST00000642271.1:c.4196-7C= ENSP00000493749.1:n.4196-7C=
ENST00000642579.1:c.2253-7C=
ENST00000642611.1:n.5410C=
ENST00000642902.1:c.3981-7C=
ENST00000643260.1:c.4199-7C= ENSP00000494450.1:n.4199-7C=
ENST00000643562.1:c.*2321-7C= ENSP00000496124.1:n.*2321-7C=
ENST00000643925.1:c.2839-7C=
ENST00000644057.1:n.276-7C=
ENST00000644484.1:c.*3585-7C= ENSP00000493558.1:n.*3585-7C=
ENST00000644675.1:c.*2371-7C= ENSP00000494567.1:n.*2371-7C=
ENST00000644757.1:c.*3202+539C= ENSP00000495085.1:n.*3202+539C=
ENST00000644772.1:c.4265-7C= ENSP00000494321.1:n.4265-7C=
ENST00000645004.1:n.1892-7C=
ENST00000645076.1:c.3398-7C=
ENST00000645417.1:c.1387-7C=
ENST00000645744.1:c.*3964-87C= ENSP00000494564.1:n.*3964-87C=
ENST00000645760.1:c.4620-7C=
ENST00000645884.1:c.*1482-7C= ENSP00000495516.1:n.*1482-7C=
ENST00000646003.1:c.*2301-87C= ENSP00000495259.1:n.*2301-87C=
ENST00000646207.1:c.*3036-7C= ENSP00000495025.1:n.*3036-7C=
ENST00000646276.1:c.*3603-7C= ENSP00000496070.1:n.*3603-7C=
ENST00000646592.1:c.3505-7C=
ENST00000646902.1:c.4166-7C= ENSP00000494101.1:n.4166-7C=
ENST00000646993.1:c.*2741-7C= ENSP00000493720.1:n.*2741-7C=
ENST00000647013.1:c.4205-7C= ENSP00000496741.1:n.4205-7C=
ENST00000647015.1:c.3950-7C= ENSP00000495389.1:n.3950-7C=
ENST00000647086.1:c.*3785-7C= ENSP00000493677.1:n.*3785-7C=
ENST00000647158.1:c.*2486-7C= ENSP00000495744.1:n.*2486-7C=
ENST00000302539.8:c.4202-7C= ENSP00000303960.4:n.4202-7C=
ENST00000389817.7:c.4199-7C= ENSP00000374467.3:n.4199-7C=
ENST00000525022.1:n.191C=
ENST00000526037.5:n.56C=
ENST00000526168.5:c.67-87C=
ENST00000531642.5:c.35-7C=
NM_000352.4:c.4199-7C= NP_000343.2:n.4199-7C=
NM_001287174.1:c.4202-7C= NP_001274103.1:n.4202-7C=
XM_011520331.1:c.4199-7C= XP_011518633.1:n.4199-7C=
XM_011520332.1:c.4202-7C= XP_011518634.1:n.4202-7C=
XM_011520333.1:c.2699-7C= XP_011518635.1:n.2699-7C=
XR_930890.1:n.4265-7C=
NM_001351295.1:c.4265-7C= NP_001338224.1:n.4265-7C=
NM_001351296.1:c.4199-7C= NP_001338225.1:n.4199-7C=
NM_001351297.1:c.4196-7C= NP_001338226.1:n.4196-7C=
NR_147094.1:n.4494-7C=
XM_017018197.2:c.4268-7C= XP_016873686.1:n.4268-7C=
XM_017018199.1:c.4265-7C= XP_016873688.1:n.4265-7C=
XM_017018201.2:c.4268-7C= XP_016873690.1:n.4268-7C=
XM_017018202.1:c.2765-7C= XP_016873691.1:n.2765-7C=
XM_017018204.1:c.2156-7C= XP_016873693.1:n.2156-7C=
XM_024448668.1:c.2567-7C= XP_024304436.1:n.2567-7C=
XR_001747945.2:n.4340-7C=
XR_001747946.2:n.4271-7C=
XR_002957189.1:n.6047C=
NM_000352.6:c.4199-7C= MANE Select NP_000343.2:n.4199-7C=
NM_001287174.2:c.4202-7C= NP_001274103.1:n.4202-7C=
NM_001351295.2:c.4265-7C= NP_001338224.1:n.4265-7C=
NM_001351296.2:c.4199-7C= NP_001338225.1:n.4199-7C=
NM_001351297.2:c.4196-7C= NP_001338226.1:n.4196-7C=
NR_147094.2:n.4494-7C=
NM_001287174.3:c.4202-7C= NP_001274103.1:n.4202-7C=