Canonical Allele Identifier: CA1955122545
Gene: ABCC8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17394269G= , CM000673.2:g.17394269G= GRCh38
NC_000011.9:g.17415816G= , CM000673.1:g.17415816G= GRCh37
NC_000011.8:g.17372392G= NCBI36
NG_008867.1:g.87634C=

Transcript Alleles

HGVS Amino-acid change
ENST00000524561.2:n.4143C=
ENST00000526037.6:n.477C=
ENST00000528374.2:c.1133C=
ENST00000529967.6:n.2881C=
ENST00000532220.2:n.3775C=
ENST00000642611.2:n.5875C=
ENST00000644057.2:n.1118C=
ENST00000645004.2:n.2041C=
ENST00000682051.1:n.4704C=
ENST00000682110.1:n.4757C=
ENST00000682140.1:c.*328C= ENSP00000507829.1:n.*328C=
ENST00000682185.1:n.5847C=
ENST00000682204.1:c.*2680C= ENSP00000507094.1:n.*2680C=
ENST00000682215.1:n.5124C=
ENST00000682288.1:c.*2973C= ENSP00000507506.1:n.*2973C=
ENST00000682442.1:n.4977C=
ENST00000682528.1:n.4834C=
ENST00000682673.1:n.4701C=
ENST00000682805.1:n.5162C=
ENST00000682965.1:c.*964C= ENSP00000508229.1:n.*964C=
ENST00000683093.1:n.5737C=
ENST00000683136.1:c.4425C= ENSP00000507768.1:p.Ala1475=
ENST00000683153.1:n.4799C=
ENST00000683365.1:n.4859C=
ENST00000683377.1:n.4653C=
ENST00000683456.1:c.*1679C= ENSP00000508318.1:n.*1679C=
ENST00000683522.1:n.4839C=
ENST00000683562.1:c.*2607C= ENSP00000508265.1:n.*2607C=
ENST00000683693.1:n.6218C=
ENST00000683725.1:c.*7C= ENSP00000507496.1:n.*7C=
ENST00000684010.1:n.4752C=
ENST00000684014.1:n.729C=
ENST00000684157.1:n.5742C=
ENST00000684253.1:n.4660C=
ENST00000684288.1:c.*2714C= ENSP00000507143.1:n.*2714C=
ENST00000684313.1:n.4189C=
ENST00000684332.1:n.4830C=
ENST00000684371.1:n.4863C=
ENST00000684404.1:n.5785C=
ENST00000684442.1:n.4981C=
ENST00000684555.1:c.*2754C= ENSP00000507705.1:n.*2754C=
ENST00000684571.1:c.4383C= ENSP00000506935.1:p.Ala1461=
ENST00000684593.1:c.*4247C= ENSP00000507005.1:n.*4247C=
ENST00000684711.1:c.*2938C= ENSP00000506841.1:n.*2938C=
ENST00000302539.9:c.4545C= ENSP00000303960.4:p.Ala1515=
ENST00000389817.8:c.4542C= MANE Select ENSP00000374467.4:p.Ala1514=
ENST00000642271.1:c.4539C= ENSP00000493749.1:p.Ala1513=
ENST00000642579.1:c.2596C=
ENST00000642611.1:n.5760C=
ENST00000642902.1:c.4324C=
ENST00000643260.1:c.4542C= ENSP00000494450.1:p.Ala1514=
ENST00000643562.1:c.*2664C= ENSP00000496124.1:n.*2664C=
ENST00000643925.1:c.3182C=
ENST00000644057.1:n.701C=
ENST00000644484.1:c.*3928C= ENSP00000493558.1:n.*3928C=
ENST00000644675.1:c.*2714C= ENSP00000494567.1:n.*2714C=
ENST00000644757.1:c.*3203-1289C= ENSP00000495085.1:n.*3203-1289C=
ENST00000644772.1:c.4608C= ENSP00000494321.1:p.Ala1536=
ENST00000645004.1:n.2235C=
ENST00000645076.1:c.3637C=
ENST00000645417.1:c.1730C=
ENST00000645744.1:c.*4227C= ENSP00000494564.1:n.*4227C=
ENST00000645760.1:c.4963C=
ENST00000645884.1:c.*1825C= ENSP00000495516.1:n.*1825C=
ENST00000646003.1:c.*2564C= ENSP00000495259.1:n.*2564C=
ENST00000646207.1:c.*3379C= ENSP00000495025.1:n.*3379C=
ENST00000646276.1:c.*3946C= ENSP00000496070.1:n.*3946C=
ENST00000646592.1:c.3848C=
ENST00000646902.1:c.4509C= ENSP00000494101.1:p.Ala1503=
ENST00000646993.1:c.*2980C= ENSP00000493720.1:n.*2980C=
ENST00000647015.1:c.4293C= ENSP00000495389.1:p.Ala1431=
ENST00000647086.1:c.*4128C= ENSP00000493677.1:n.*4128C=
ENST00000647158.1:c.*2829C= ENSP00000495744.1:n.*2829C=
ENST00000302539.8:c.4545C= ENSP00000303960.4:p.Ala1515=
ENST00000389817.7:c.4542C= ENSP00000374467.3:p.Ala1514=
ENST00000525022.1:n.437C=
ENST00000526037.5:n.302C=
ENST00000526168.5:c.330C=
ENST00000531642.5:c.573C=
NM_000352.4:c.4542C= NP_000343.2:p.Ala1514=
NM_001287174.1:c.4545C= NP_001274103.1:p.Ala1515=
XM_011520331.1:c.4542C= XP_011518633.1:p.Ala1514=
XM_011520332.1:c.*7C= XP_011518634.1:n.*7C=
XM_011520333.1:c.3042C= XP_011518635.1:p.Ala1014=
XR_930890.1:n.4504C=
NM_001351295.1:c.4608C= NP_001338224.1:p.Ala1536=
NM_001351296.1:c.4542C= NP_001338225.1:p.Ala1514=
NM_001351297.1:c.4539C= NP_001338226.1:p.Ala1513=
NR_147094.1:n.4837C=
XM_017018197.2:c.4611C= XP_016873686.1:p.Ala1537=
XM_017018199.1:c.4608C= XP_016873688.1:p.Ala1536=
XM_017018201.2:c.*7C= XP_016873690.1:n.*7C=
XM_017018202.1:c.3108C= XP_016873691.1:p.Ala1036=
XM_017018204.1:c.2499C= XP_016873693.1:p.Ala833=
XM_024448668.1:c.2910C= XP_024304436.1:p.Ala970=
XR_001747945.2:n.4579C=
XR_001747946.2:n.4510C=
XR_002957189.1:n.6293C=
NM_000352.6:c.4542C= MANE Select NP_000343.2:p.Ala1514=
NM_001287174.2:c.4545C= NP_001274103.1:p.Ala1515=
NM_001351295.2:c.4608C= NP_001338224.1:p.Ala1536=
NM_001351296.2:c.4542C= NP_001338225.1:p.Ala1514=
NM_001351297.2:c.4539C= NP_001338226.1:p.Ala1513=
NR_147094.2:n.4837C=
NM_001287174.3:c.4545C= NP_001274103.1:p.Ala1515=