Canonical Allele Identifier: CA1955123249
Gene: ABCC8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17395678C= , CM000673.2:g.17395678C= GRCh38
NC_000011.9:g.17417225C= , CM000673.1:g.17417225C= GRCh37
NC_000011.8:g.17373801C= NCBI36
NG_008867.1:g.86225G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000524561.2:n.3840G=
ENST00000528374.2:c.830G=
ENST00000529967.6:n.2578G=
ENST00000532220.2:n.3472G=
ENST00000642611.2:n.5572G=
ENST00000644057.2:n.815G=
ENST00000645004.2:n.1738G=
ENST00000682051.1:n.4401G=
ENST00000682110.1:n.4454G=
ENST00000682140.1:c.*25G= ENSP00000507829.1:n.*25G=
ENST00000682185.1:n.5544G=
ENST00000682204.1:c.*2377G= ENSP00000507094.1:n.*2377G=
ENST00000682215.1:n.4821G=
ENST00000682288.1:c.*2670G= ENSP00000507506.1:n.*2670G=
ENST00000682442.1:n.4674G=
ENST00000682528.1:n.4531G=
ENST00000682673.1:n.4398G=
ENST00000682805.1:n.4859G=
ENST00000682965.1:c.*661G= ENSP00000508229.1:n.*661G=
ENST00000683093.1:n.5538G=
ENST00000683136.1:c.4122G= ENSP00000507768.1:p.Pro1374=
ENST00000683153.1:n.4496G=
ENST00000683365.1:n.4556G=
ENST00000683377.1:n.4454G=
ENST00000683456.1:c.*1376G= ENSP00000508318.1:n.*1376G=
ENST00000683522.1:n.4454G=
ENST00000683562.1:c.*2408G= ENSP00000508265.1:n.*2408G=
ENST00000683693.1:n.6019G=
ENST00000683725.1:c.4239G= ENSP00000507496.1:p.Pro1413=
ENST00000684010.1:n.4449G=
ENST00000684157.1:n.5439G=
ENST00000684253.1:n.4357G=
ENST00000684288.1:c.*2411G= ENSP00000507143.1:n.*2411G=
ENST00000684313.1:n.3886G=
ENST00000684332.1:n.4527G=
ENST00000684371.1:n.4560G=
ENST00000684404.1:n.5482G=
ENST00000684442.1:n.4678G=
ENST00000684555.1:c.*2451G= ENSP00000507705.1:n.*2451G=
ENST00000684571.1:c.4080G= ENSP00000506935.1:p.Pro1360=
ENST00000684593.1:c.*3944G= ENSP00000507005.1:n.*3944G=
ENST00000684711.1:c.*2635G= ENSP00000506841.1:n.*2635G=
ENST00000302539.9:c.4242G= ENSP00000303960.4:p.Pro1414=
ENST00000389817.8:c.4239G= MANE Select ENSP00000374467.4:p.Pro1413=
ENST00000642271.1:c.4236G= ENSP00000493749.1:p.Pro1412=
ENST00000642579.1:c.2293G=
ENST00000642611.1:n.5457G=
ENST00000642902.1:c.4021G=
ENST00000643260.1:c.4239G= ENSP00000494450.1:p.Pro1413=
ENST00000643562.1:c.*2361G= ENSP00000496124.1:n.*2361G=
ENST00000643925.1:c.2879G=
ENST00000644057.1:n.316G=
ENST00000644484.1:c.*3625G= ENSP00000493558.1:n.*3625G=
ENST00000644675.1:c.*2411G= ENSP00000494567.1:n.*2411G=
ENST00000644757.1:c.*3202+586G= ENSP00000495085.1:n.*3202+586G=
ENST00000644772.1:c.4305G= ENSP00000494321.1:p.Pro1435=
ENST00000645004.1:n.1932G=
ENST00000645076.1:c.3438G=
ENST00000645417.1:c.1427G=
ENST00000645744.1:c.*3964-40G= ENSP00000494564.1:n.*3964-40G=
ENST00000645760.1:c.4660G=
ENST00000645884.1:c.*1522G= ENSP00000495516.1:n.*1522G=
ENST00000646003.1:c.*2301-40G= ENSP00000495259.1:n.*2301-40G=
ENST00000646207.1:c.*3076G= ENSP00000495025.1:n.*3076G=
ENST00000646276.1:c.*3643G= ENSP00000496070.1:n.*3643G=
ENST00000646592.1:c.3545G=
ENST00000646902.1:c.4206G= ENSP00000494101.1:p.Pro1402=
ENST00000646993.1:c.*2781G= ENSP00000493720.1:n.*2781G=
ENST00000647013.1:c.4245G= ENSP00000496741.1:n.4245G=
ENST00000647015.1:c.3990G= ENSP00000495389.1:p.Pro1330=
ENST00000647086.1:c.*3825G= ENSP00000493677.1:n.*3825G=
ENST00000647158.1:c.*2526G= ENSP00000495744.1:n.*2526G=
ENST00000302539.8:c.4242G= ENSP00000303960.4:p.Pro1414=
ENST00000389817.7:c.4239G= ENSP00000374467.3:p.Pro1413=
ENST00000525022.1:n.238G=
ENST00000526037.5:n.103G=
ENST00000526168.5:c.67-40G=
ENST00000531642.5:c.75G=
NM_000352.4:c.4239G= NP_000343.2:p.Pro1413=
NM_001287174.1:c.4242G= NP_001274103.1:p.Pro1414=
XM_011520331.1:c.4239G= XP_011518633.1:p.Pro1413=
XM_011520332.1:c.4242G= XP_011518634.1:p.Pro1414=
XM_011520333.1:c.2739G= XP_011518635.1:p.Pro913=
XR_930890.1:n.4305G=
NM_001351295.1:c.4305G= NP_001338224.1:p.Pro1435=
NM_001351296.1:c.4239G= NP_001338225.1:p.Pro1413=
NM_001351297.1:c.4236G= NP_001338226.1:p.Pro1412=
NR_147094.1:n.4534G=
XM_017018197.2:c.4308G= XP_016873686.1:p.Pro1436=
XM_017018199.1:c.4305G= XP_016873688.1:p.Pro1435=
XM_017018201.2:c.4308G= XP_016873690.1:p.Pro1436=
XM_017018202.1:c.2805G= XP_016873691.1:p.Pro935=
XM_017018204.1:c.2196G= XP_016873693.1:p.Pro732=
XM_024448668.1:c.2607G= XP_024304436.1:p.Pro869=
XR_001747945.2:n.4380G=
XR_001747946.2:n.4311G=
XR_002957189.1:n.6094G=
NM_000352.6:c.4239G= MANE Select NP_000343.2:p.Pro1413=
NM_001287174.2:c.4242G= NP_001274103.1:p.Pro1414=
NM_001351295.2:c.4305G= NP_001338224.1:p.Pro1435=
NM_001351296.2:c.4239G= NP_001338225.1:p.Pro1413=
NM_001351297.2:c.4236G= NP_001338226.1:p.Pro1412=
NR_147094.2:n.4534G=
NM_001287174.3:c.4242G= NP_001274103.1:p.Pro1414=