Canonical Allele Identifier: CA1955122292
Gene: ABCC8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17393700G= , CM000673.2:g.17393700G= GRCh38
NC_000011.9:g.17415247G= , CM000673.1:g.17415247G= GRCh37
NC_000011.8:g.17371823G= NCBI36
NG_008867.1:g.88203C=

Transcript Alleles

HGVS Amino-acid change
ENST00000524561.2:n.4206C=
ENST00000526037.6:n.540C=
ENST00000528374.2:c.1196C=
ENST00000529967.6:n.2944C=
ENST00000532220.2:n.3838C=
ENST00000642611.2:n.5938C=
ENST00000644057.2:n.1181C=
ENST00000645004.2:n.2104C=
ENST00000682051.1:n.4767C=
ENST00000682110.1:n.4820C=
ENST00000682140.1:c.*391C= ENSP00000507829.1:n.*391C=
ENST00000682185.1:n.5910C=
ENST00000682204.1:c.*2743C= ENSP00000507094.1:n.*2743C=
ENST00000682215.1:n.5187C=
ENST00000682288.1:c.*3036C= ENSP00000507506.1:n.*3036C=
ENST00000682442.1:n.5040C=
ENST00000682528.1:n.4897C=
ENST00000682673.1:n.4764C=
ENST00000682805.1:n.5225C=
ENST00000682965.1:c.*1027C= ENSP00000508229.1:n.*1027C=
ENST00000683093.1:n.5800C=
ENST00000683136.1:c.4488C= ENSP00000507768.1:p.Ile1496=
ENST00000683153.1:n.4862C=
ENST00000683365.1:n.4922C=
ENST00000683377.1:n.4716C=
ENST00000683456.1:c.*1742C= ENSP00000508318.1:n.*1742C=
ENST00000683522.1:n.4902C=
ENST00000683562.1:c.*2670C= ENSP00000508265.1:n.*2670C=
ENST00000683693.1:n.6281C=
ENST00000683725.1:c.*70C= ENSP00000507496.1:n.*70C=
ENST00000684010.1:n.4815C=
ENST00000684014.1:n.792C=
ENST00000684157.1:n.5805C=
ENST00000684253.1:n.4723C=
ENST00000684288.1:c.*2777C= ENSP00000507143.1:n.*2777C=
ENST00000684313.1:n.4252C=
ENST00000684332.1:n.4893C=
ENST00000684371.1:n.4926C=
ENST00000684404.1:n.5848C=
ENST00000684442.1:n.5044C=
ENST00000684555.1:c.*2817C= ENSP00000507705.1:n.*2817C=
ENST00000684571.1:c.4446C= ENSP00000506935.1:p.Ile1482=
ENST00000684593.1:c.*4310C= ENSP00000507005.1:n.*4310C=
ENST00000684711.1:c.*3001C= ENSP00000506841.1:n.*3001C=
ENST00000302539.9:c.4608C= ENSP00000303960.4:p.Ile1536=
ENST00000389817.8:c.4605C= MANE Select ENSP00000374467.4:p.Ile1535=
ENST00000642271.1:c.4602C= ENSP00000493749.1:p.Ile1534=
ENST00000642579.1:c.2659C=
ENST00000642611.1:n.5823C=
ENST00000642902.1:c.4387C=
ENST00000643260.1:c.4605C= ENSP00000494450.1:p.Ile1535=
ENST00000643562.1:c.*2727C= ENSP00000496124.1:n.*2727C=
ENST00000643925.1:c.3185+566C=
ENST00000644057.1:n.764C=
ENST00000644484.1:c.*3991C= ENSP00000493558.1:n.*3991C=
ENST00000644675.1:c.*2777C= ENSP00000494567.1:n.*2777C=
ENST00000644757.1:c.*3203-720C= ENSP00000495085.1:n.*3203-720C=
ENST00000644772.1:c.4671C= ENSP00000494321.1:p.Ile1557=
ENST00000645004.1:n.2298C=
ENST00000645076.1:c.3700C=
ENST00000645417.1:c.1793C=
ENST00000645744.1:c.*4290C= ENSP00000494564.1:n.*4290C=
ENST00000645760.1:c.5026C=
ENST00000645884.1:c.*1888C= ENSP00000495516.1:n.*1888C=
ENST00000646003.1:c.*2627C= ENSP00000495259.1:n.*2627C=
ENST00000646207.1:c.*3442C= ENSP00000495025.1:n.*3442C=
ENST00000646276.1:c.*4009C= ENSP00000496070.1:n.*4009C=
ENST00000646592.1:c.3911C=
ENST00000646902.1:c.4572C= ENSP00000494101.1:p.Ile1524=
ENST00000646993.1:c.*3043C= ENSP00000493720.1:n.*3043C=
ENST00000647015.1:c.4356C= ENSP00000495389.1:p.Ile1452=
ENST00000647086.1:c.*4191C= ENSP00000493677.1:n.*4191C=
ENST00000647158.1:c.*2892C= ENSP00000495744.1:n.*2892C=
ENST00000302539.8:c.4608C= ENSP00000303960.4:p.Ile1536=
ENST00000389817.7:c.4605C= ENSP00000374467.3:p.Ile1535=
ENST00000525022.1:n.500C=
ENST00000526037.5:n.365C=
ENST00000526168.5:c.393C=
ENST00000531642.5:c.636C=
NM_000352.4:c.4605C= NP_000343.2:p.Ile1535=
NM_001287174.1:c.4608C= NP_001274103.1:p.Ile1536=
XM_011520331.1:c.4605C= XP_011518633.1:p.Ile1535=
XM_011520333.1:c.3105C= XP_011518635.1:p.Ile1035=
XR_930890.1:n.4567C=
NM_001351295.1:c.4671C= NP_001338224.1:p.Ile1557=
NM_001351296.1:c.4605C= NP_001338225.1:p.Ile1535=
NM_001351297.1:c.4602C= NP_001338226.1:p.Ile1534=
NR_147094.1:n.4900C=
XM_017018197.2:c.4674C= XP_016873686.1:p.Ile1558=
XM_017018199.1:c.4671C= XP_016873688.1:p.Ile1557=
XM_017018202.1:c.3171C= XP_016873691.1:p.Ile1057=
XM_017018204.1:c.2562C= XP_016873693.1:p.Ile854=
XM_024448668.1:c.2973C= XP_024304436.1:p.Ile991=
XR_001747945.2:n.4642C=
XR_001747946.2:n.4573C=
XR_002957189.1:n.6356C=
NM_000352.6:c.4605C= MANE Select NP_000343.2:p.Ile1535=
NM_001287174.2:c.4608C= NP_001274103.1:p.Ile1536=
NM_001351295.2:c.4671C= NP_001338224.1:p.Ile1557=
NM_001351296.2:c.4605C= NP_001338225.1:p.Ile1535=
NM_001351297.2:c.4602C= NP_001338226.1:p.Ile1534=
NR_147094.2:n.4900C=
NM_001287174.3:c.4608C= NP_001274103.1:p.Ile1536=