Canonical Allele Identifier: CA1955123340
Gene: ABCC8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17395862G= , CM000673.2:g.17395862G= GRCh38
NC_000011.9:g.17417409G= , CM000673.1:g.17417409G= GRCh37
NC_000011.8:g.17373985G= NCBI36
NG_008867.1:g.86041C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000524561.2:n.3789C=
ENST00000528374.2:c.779C=
ENST00000529967.6:n.2527C=
ENST00000532220.2:n.3421C=
ENST00000642611.2:n.5388C=
ENST00000644057.2:n.631C=
ENST00000645004.2:n.1687C=
ENST00000682051.1:n.4350C=
ENST00000682110.1:n.4403C=
ENST00000682140.1:c.4054C= ENSP00000507829.1:p.His1352=
ENST00000682185.1:n.5493C=
ENST00000682204.1:c.*2326C= ENSP00000507094.1:n.*2326C=
ENST00000682215.1:n.4770C=
ENST00000682288.1:c.*2619C= ENSP00000507506.1:n.*2619C=
ENST00000682442.1:n.4623C=
ENST00000682528.1:n.4480C=
ENST00000682673.1:n.4347C=
ENST00000682805.1:n.4808C=
ENST00000682965.1:c.*610C= ENSP00000508229.1:n.*610C=
ENST00000683093.1:n.5487C=
ENST00000683136.1:c.4071C= ENSP00000507768.1:p.Asp1357=
ENST00000683153.1:n.4445C=
ENST00000683365.1:n.4505C=
ENST00000683377.1:n.4403C=
ENST00000683456.1:c.*1325C= ENSP00000508318.1:n.*1325C=
ENST00000683522.1:n.4403C=
ENST00000683562.1:c.*2357C= ENSP00000508265.1:n.*2357C=
ENST00000683693.1:n.5835C=
ENST00000683725.1:c.4188C= ENSP00000507496.1:p.Asp1396=
ENST00000684010.1:n.4398C=
ENST00000684157.1:n.5388C=
ENST00000684253.1:n.4306C=
ENST00000684288.1:c.*2360C= ENSP00000507143.1:n.*2360C=
ENST00000684313.1:n.3835C=
ENST00000684332.1:n.4476C=
ENST00000684371.1:n.4509C=
ENST00000684404.1:n.5431C=
ENST00000684442.1:n.4627C=
ENST00000684555.1:c.*2400C= ENSP00000507705.1:n.*2400C=
ENST00000684571.1:c.4029C= ENSP00000506935.1:p.Asp1343=
ENST00000684593.1:c.*3893C= ENSP00000507005.1:n.*3893C=
ENST00000684711.1:c.*2584C= ENSP00000506841.1:n.*2584C=
ENST00000302539.9:c.4191C= ENSP00000303960.4:p.Asp1397=
ENST00000389817.8:c.4188C= MANE Select ENSP00000374467.4:p.Asp1396=
ENST00000642271.1:c.4185C= ENSP00000493749.1:p.Asp1395=
ENST00000642579.1:c.2242C=
ENST00000642611.1:n.5273C=
ENST00000642902.1:c.3970C=
ENST00000643260.1:c.4188C= ENSP00000494450.1:p.Asp1396=
ENST00000643562.1:c.*2310C= ENSP00000496124.1:n.*2310C=
ENST00000643925.1:c.2828C=
ENST00000644057.1:n.265C=
ENST00000644484.1:c.*3574C= ENSP00000493558.1:n.*3574C=
ENST00000644675.1:c.*2360C= ENSP00000494567.1:n.*2360C=
ENST00000644757.1:c.*3202+402C= ENSP00000495085.1:n.*3202+402C=
ENST00000644772.1:c.4254C= ENSP00000494321.1:p.Asp1418=
ENST00000645004.1:n.1881C=
ENST00000645076.1:c.3387C=
ENST00000645417.1:c.1376C=
ENST00000645744.1:c.*3953C= ENSP00000494564.1:n.*3953C=
ENST00000645760.1:c.4609C=
ENST00000645884.1:c.*1471C= ENSP00000495516.1:n.*1471C=
ENST00000646003.1:c.*2290C= ENSP00000495259.1:n.*2290C=
ENST00000646207.1:c.*3025C= ENSP00000495025.1:n.*3025C=
ENST00000646276.1:c.*3592C= ENSP00000496070.1:n.*3592C=
ENST00000646592.1:c.3494C=
ENST00000646902.1:c.4155C= ENSP00000494101.1:p.Asp1385=
ENST00000646993.1:c.*2730C= ENSP00000493720.1:n.*2730C=
ENST00000647013.1:c.4194C= ENSP00000496741.1:n.4194C=
ENST00000647015.1:c.3939C= ENSP00000495389.1:p.Asp1313=
ENST00000647086.1:c.*3774C= ENSP00000493677.1:n.*3774C=
ENST00000647158.1:c.*2475C= ENSP00000495744.1:n.*2475C=
ENST00000302539.8:c.4191C= ENSP00000303960.4:p.Asp1397=
ENST00000389817.7:c.4188C= ENSP00000374467.3:p.Asp1396=
ENST00000525022.1:n.54C=
ENST00000526168.5:c.56C=
ENST00000531642.5:c.24C=
NM_000352.4:c.4188C= NP_000343.2:p.Asp1396=
NM_001287174.1:c.4191C= NP_001274103.1:p.Asp1397=
XM_011520331.1:c.4188C= XP_011518633.1:p.Asp1396=
XM_011520332.1:c.4191C= XP_011518634.1:p.Asp1397=
XM_011520333.1:c.2688C= XP_011518635.1:p.Asp896=
XR_930890.1:n.4254C=
NM_001351295.1:c.4254C= NP_001338224.1:p.Asp1418=
NM_001351296.1:c.4188C= NP_001338225.1:p.Asp1396=
NM_001351297.1:c.4185C= NP_001338226.1:p.Asp1395=
NR_147094.1:n.4483C=
XM_017018197.2:c.4257C= XP_016873686.1:p.Asp1419=
XM_017018199.1:c.4254C= XP_016873688.1:p.Asp1418=
XM_017018201.2:c.4257C= XP_016873690.1:p.Asp1419=
XM_017018202.1:c.2754C= XP_016873691.1:p.Asp918=
XM_017018204.1:c.2145C= XP_016873693.1:p.Asp715=
XM_024448668.1:c.2556C= XP_024304436.1:p.Asp852=
XR_001747945.2:n.4329C=
XR_001747946.2:n.4260C=
XR_002957189.1:n.5910C=
NM_000352.6:c.4188C= MANE Select NP_000343.2:p.Asp1396=
NM_001287174.2:c.4191C= NP_001274103.1:p.Asp1397=
NM_001351295.2:c.4254C= NP_001338224.1:p.Asp1418=
NM_001351296.2:c.4188C= NP_001338225.1:p.Asp1396=
NM_001351297.2:c.4185C= NP_001338226.1:p.Asp1395=
NR_147094.2:n.4483C=
NM_001287174.3:c.4191C= NP_001274103.1:p.Asp1397=