Canonical Allele Identifier: CA1955127513
Gene: ABCC8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17404452C= , CM000673.2:g.17404452C= GRCh38
NC_000011.9:g.17425999C= , CM000673.1:g.17425999C= GRCh37
NC_000011.8:g.17382575C= NCBI36
NG_008867.1:g.77451G=

Transcript Alleles

HGVS Amino-acid change
ENST00000524561.2:n.3126+60G=
ENST00000528374.2:c.136+60G=
ENST00000529967.6:n.1896+60G=
ENST00000532220.2:n.1289+60G=
ENST00000642611.2:n.3626+60G=
ENST00000645004.2:n.1056+60G=
ENST00000682051.1:n.3573+60G=
ENST00000682110.1:n.3626+60G=
ENST00000682140.1:c.3554+60G= ENSP00000507829.1:n.3554+60G=
ENST00000682185.1:n.4862+60G=
ENST00000682204.1:c.*1695+60G= ENSP00000507094.1:n.*1695+60G=
ENST00000682215.1:n.3623+60G=
ENST00000682288.1:c.*1988+60G= ENSP00000507506.1:n.*1988+60G=
ENST00000682442.1:n.3846+60G=
ENST00000682528.1:n.3703+60G=
ENST00000682673.1:n.3570+60G=
ENST00000682805.1:n.3623+60G=
ENST00000682965.1:c.3396+1042G= ENSP00000508229.1:n.3396+1042G=
ENST00000683093.1:n.3725+60G=
ENST00000683136.1:c.3554+60G= ENSP00000507768.1:n.3554+60G=
ENST00000683153.1:n.3782+60G=
ENST00000683365.1:n.3728+60G=
ENST00000683377.1:n.3626+60G=
ENST00000683456.1:c.*694+60G= ENSP00000508318.1:n.*694+60G=
ENST00000683522.1:n.3626+60G=
ENST00000683562.1:c.*1726+60G= ENSP00000508265.1:n.*1726+60G=
ENST00000683693.1:n.3703+60G=
ENST00000683725.1:c.3557+60G= ENSP00000507496.1:n.3557+60G=
ENST00000684010.1:n.3621+60G=
ENST00000684157.1:n.3626+60G=
ENST00000684253.1:n.3529+60G=
ENST00000684288.1:c.*1729+60G= ENSP00000507143.1:n.*1729+60G=
ENST00000684313.1:n.3058+60G=
ENST00000684332.1:n.3699+60G=
ENST00000684371.1:n.3732+60G=
ENST00000684404.1:n.3669+60G=
ENST00000684442.1:n.3626+60G=
ENST00000684555.1:c.*1769+60G= ENSP00000507705.1:n.*1769+60G=
ENST00000684571.1:c.3398+60G= ENSP00000506935.1:n.3398+60G=
ENST00000684593.1:c.*3262+60G= ENSP00000507005.1:n.*3262+60G=
ENST00000684711.1:c.*1953+60G= ENSP00000506841.1:n.*1953+60G=
ENST00000302539.9:c.3560+60G= ENSP00000303960.4:n.3560+60G=
ENST00000389817.8:c.3557+60G= MANE Select ENSP00000374467.4:n.3557+60G=
ENST00000642271.1:c.3554+60G= ENSP00000493749.1:n.3554+60G=
ENST00000642579.1:c.1641+60G=
ENST00000642611.1:n.3511+60G=
ENST00000642902.1:c.3339+60G=
ENST00000643260.1:c.3557+60G= ENSP00000494450.1:n.3557+60G=
ENST00000643562.1:c.*1533+60G= ENSP00000496124.1:n.*1533+60G=
ENST00000643925.1:c.1681+60G=
ENST00000644447.1:c.1913+60G= ENSP00000496282.1:n.1913+60G=
ENST00000644484.1:c.*1812+60G= ENSP00000493558.1:n.*1812+60G=
ENST00000644675.1:c.*1729+60G= ENSP00000494567.1:n.*1729+60G=
ENST00000644757.1:c.*1842+60G= ENSP00000495085.1:n.*1842+60G=
ENST00000644772.1:c.3623+60G= ENSP00000494321.1:n.3623+60G=
ENST00000645004.1:n.696+60G=
ENST00000645076.1:c.2756+60G=
ENST00000645417.1:c.723+60G=
ENST00000645744.1:c.*1821+60G= ENSP00000494564.1:n.*1821+60G=
ENST00000645760.1:c.3832+60G=
ENST00000645884.1:c.*694+60G= ENSP00000495516.1:n.*694+60G=
ENST00000646003.1:c.*1513+60G= ENSP00000495259.1:n.*1513+60G=
ENST00000646207.1:c.*2024+60G= ENSP00000495025.1:n.*2024+60G=
ENST00000646276.1:c.*1830+60G= ENSP00000496070.1:n.*1830+60G=
ENST00000646592.1:c.2863+60G=
ENST00000646902.1:c.3554+60G= ENSP00000494101.1:n.3554+60G=
ENST00000646993.1:c.*1953+60G= ENSP00000493720.1:n.*1953+60G=
ENST00000647013.1:c.3563+60G= ENSP00000496741.1:n.3563+60G=
ENST00000647015.1:c.3308+60G= ENSP00000495389.1:n.3308+60G=
ENST00000647086.1:c.*3287+60G= ENSP00000493677.1:n.*3287+60G=
ENST00000647158.1:c.*1698+60G= ENSP00000495744.1:n.*1698+60G=
ENST00000302539.8:c.3560+60G= ENSP00000303960.4:n.3560+60G=
ENST00000389817.7:c.3557+60G= ENSP00000374467.3:n.3557+60G=
ENST00000524561.1:n.689+60G=
ENST00000527905.5:c.*433+60G= ENSP00000431653.1:n.*433+60G=
ENST00000528374.1:c.27+60G=
ENST00000531137.1:n.50+60G=
NM_000352.4:c.3557+60G= NP_000343.2:n.3557+60G=
NM_001287174.1:c.3560+60G= NP_001274103.1:n.3560+60G=
XM_011520331.1:c.3557+60G= XP_011518633.1:n.3557+60G=
XM_011520332.1:c.3560+60G= XP_011518634.1:n.3560+60G=
XM_011520333.1:c.2057+60G= XP_011518635.1:n.2057+60G=
XR_930890.1:n.3623+60G=
XR_930892.1:n.3523+60G=
XR_930893.1:n.3520+60G=
NM_001351295.1:c.3623+60G= NP_001338224.1:n.3623+60G=
NM_001351296.1:c.3557+60G= NP_001338225.1:n.3557+60G=
NM_001351297.1:c.3554+60G= NP_001338226.1:n.3554+60G=
NR_147094.1:n.3706+60G=
XM_017018197.2:c.3626+60G= XP_016873686.1:n.3626+60G=
XM_017018199.1:c.3623+60G= XP_016873688.1:n.3623+60G=
XM_017018201.2:c.3626+60G= XP_016873690.1:n.3626+60G=
XM_017018202.1:c.2123+60G= XP_016873691.1:n.2123+60G=
XM_017018204.1:c.1514+60G= XP_016873693.1:n.1514+60G=
XM_024448668.1:c.1925+60G= XP_024304436.1:n.1925+60G=
XR_001747945.2:n.3698+60G=
XR_001747946.2:n.3629+60G=
XR_002957189.1:n.3778+60G=
NM_000352.6:c.3557+60G= MANE Select NP_000343.2:n.3557+60G=
NM_001287174.2:c.3560+60G= NP_001274103.1:n.3560+60G=
NM_001351295.2:c.3623+60G= NP_001338224.1:n.3623+60G=
NM_001351296.2:c.3557+60G= NP_001338225.1:n.3557+60G=
NM_001351297.2:c.3554+60G= NP_001338226.1:n.3554+60G=
NR_147094.2:n.3706+60G=
NM_001287174.3:c.3560+60G= NP_001274103.1:n.3560+60G=