Canonical Allele Identifier: CA1955122302
Gene: ABCC8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17393723C= , CM000673.2:g.17393723C= GRCh38
NC_000011.9:g.17415270C= , CM000673.1:g.17415270C= GRCh37
NC_000011.8:g.17371846C= NCBI36
NG_008867.1:g.88180G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000524561.2:n.4183G=
ENST00000526037.6:n.517G=
ENST00000528374.2:c.1173G=
ENST00000529967.6:n.2921G=
ENST00000532220.2:n.3815G=
ENST00000642611.2:n.5915G=
ENST00000644057.2:n.1158G=
ENST00000645004.2:n.2081G=
ENST00000682051.1:n.4744G=
ENST00000682110.1:n.4797G=
ENST00000682140.1:c.*368G= ENSP00000507829.1:n.*368G=
ENST00000682185.1:n.5887G=
ENST00000682204.1:c.*2720G= ENSP00000507094.1:n.*2720G=
ENST00000682215.1:n.5164G=
ENST00000682288.1:c.*3013G= ENSP00000507506.1:n.*3013G=
ENST00000682442.1:n.5017G=
ENST00000682528.1:n.4874G=
ENST00000682673.1:n.4741G=
ENST00000682805.1:n.5202G=
ENST00000682965.1:c.*1004G= ENSP00000508229.1:n.*1004G=
ENST00000683093.1:n.5777G=
ENST00000683136.1:c.4465G= ENSP00000507768.1:p.Ala1489=
ENST00000683153.1:n.4839G=
ENST00000683365.1:n.4899G=
ENST00000683377.1:n.4693G=
ENST00000683456.1:c.*1719G= ENSP00000508318.1:n.*1719G=
ENST00000683522.1:n.4879G=
ENST00000683562.1:c.*2647G= ENSP00000508265.1:n.*2647G=
ENST00000683693.1:n.6258G=
ENST00000683725.1:c.*47G= ENSP00000507496.1:n.*47G=
ENST00000684010.1:n.4792G=
ENST00000684014.1:n.769G=
ENST00000684157.1:n.5782G=
ENST00000684253.1:n.4700G=
ENST00000684288.1:c.*2754G= ENSP00000507143.1:n.*2754G=
ENST00000684313.1:n.4229G=
ENST00000684332.1:n.4870G=
ENST00000684371.1:n.4903G=
ENST00000684404.1:n.5825G=
ENST00000684442.1:n.5021G=
ENST00000684555.1:c.*2794G= ENSP00000507705.1:n.*2794G=
ENST00000684571.1:c.4423G= ENSP00000506935.1:p.Ala1475=
ENST00000684593.1:c.*4287G= ENSP00000507005.1:n.*4287G=
ENST00000684711.1:c.*2978G= ENSP00000506841.1:n.*2978G=
ENST00000302539.9:c.4585G= ENSP00000303960.4:p.Ala1529=
ENST00000389817.8:c.4582G= MANE Select ENSP00000374467.4:p.Ala1528=
ENST00000642271.1:c.4579G= ENSP00000493749.1:p.Ala1527=
ENST00000642579.1:c.2636G=
ENST00000642611.1:n.5800G=
ENST00000642902.1:c.4364G=
ENST00000643260.1:c.4582G= ENSP00000494450.1:p.Ala1528=
ENST00000643562.1:c.*2704G= ENSP00000496124.1:n.*2704G=
ENST00000643925.1:c.3185+543G=
ENST00000644057.1:n.741G=
ENST00000644484.1:c.*3968G= ENSP00000493558.1:n.*3968G=
ENST00000644675.1:c.*2754G= ENSP00000494567.1:n.*2754G=
ENST00000644757.1:c.*3203-743G= ENSP00000495085.1:n.*3203-743G=
ENST00000644772.1:c.4648G= ENSP00000494321.1:p.Ala1550=
ENST00000645004.1:n.2275G=
ENST00000645076.1:c.3677G=
ENST00000645417.1:c.1770G=
ENST00000645744.1:c.*4267G= ENSP00000494564.1:n.*4267G=
ENST00000645760.1:c.5003G=
ENST00000645884.1:c.*1865G= ENSP00000495516.1:n.*1865G=
ENST00000646003.1:c.*2604G= ENSP00000495259.1:n.*2604G=
ENST00000646207.1:c.*3419G= ENSP00000495025.1:n.*3419G=
ENST00000646276.1:c.*3986G= ENSP00000496070.1:n.*3986G=
ENST00000646592.1:c.3888G=
ENST00000646902.1:c.4549G= ENSP00000494101.1:p.Ala1517=
ENST00000646993.1:c.*3020G= ENSP00000493720.1:n.*3020G=
ENST00000647015.1:c.4333G= ENSP00000495389.1:p.Ala1445=
ENST00000647086.1:c.*4168G= ENSP00000493677.1:n.*4168G=
ENST00000647158.1:c.*2869G= ENSP00000495744.1:n.*2869G=
ENST00000302539.8:c.4585G= ENSP00000303960.4:p.Ala1529=
ENST00000389817.7:c.4582G= ENSP00000374467.3:p.Ala1528=
ENST00000525022.1:n.477G=
ENST00000526037.5:n.342G=
ENST00000526168.5:c.370G=
ENST00000531642.5:c.613G=
NM_000352.4:c.4582G= NP_000343.2:p.Ala1528=
NM_001287174.1:c.4585G= NP_001274103.1:p.Ala1529=
XM_011520331.1:c.4582G= XP_011518633.1:p.Ala1528=
XM_011520333.1:c.3082G= XP_011518635.1:p.Ala1028=
XR_930890.1:n.4544G=
NM_001351295.1:c.4648G= NP_001338224.1:p.Ala1550=
NM_001351296.1:c.4582G= NP_001338225.1:p.Ala1528=
NM_001351297.1:c.4579G= NP_001338226.1:p.Ala1527=
NR_147094.1:n.4877G=
XM_017018197.2:c.4651G= XP_016873686.1:p.Ala1551=
XM_017018199.1:c.4648G= XP_016873688.1:p.Ala1550=
XM_017018202.1:c.3148G= XP_016873691.1:p.Ala1050=
XM_017018204.1:c.2539G= XP_016873693.1:p.Ala847=
XM_024448668.1:c.2950G= XP_024304436.1:p.Ala984=
XR_001747945.2:n.4619G=
XR_001747946.2:n.4550G=
XR_002957189.1:n.6333G=
NM_000352.6:c.4582G= MANE Select NP_000343.2:p.Ala1528=
NM_001287174.2:c.4585G= NP_001274103.1:p.Ala1529=
NM_001351295.2:c.4648G= NP_001338224.1:p.Ala1550=
NM_001351296.2:c.4582G= NP_001338225.1:p.Ala1528=
NM_001351297.2:c.4579G= NP_001338226.1:p.Ala1527=
NR_147094.2:n.4877G=
NM_001287174.3:c.4585G= NP_001274103.1:p.Ala1529=