Canonical Allele Identifier: CA1955123235
Gene: ABCC8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17395647T= , CM000673.2:g.17395647T= GRCh38
NC_000011.9:g.17417194T= , CM000673.1:g.17417194T= GRCh37
NC_000011.8:g.17373770T= NCBI36
NG_008867.1:g.86256A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000524561.2:n.3871A=
ENST00000528374.2:c.861A=
ENST00000529967.6:n.2609A=
ENST00000532220.2:n.3503A=
ENST00000642611.2:n.5603A=
ENST00000644057.2:n.846A=
ENST00000645004.2:n.1769A=
ENST00000682051.1:n.4432A=
ENST00000682110.1:n.4485A=
ENST00000682140.1:c.*56A= ENSP00000507829.1:n.*56A=
ENST00000682185.1:n.5575A=
ENST00000682204.1:c.*2408A= ENSP00000507094.1:n.*2408A=
ENST00000682215.1:n.4852A=
ENST00000682288.1:c.*2701A= ENSP00000507506.1:n.*2701A=
ENST00000682442.1:n.4705A=
ENST00000682528.1:n.4562A=
ENST00000682673.1:n.4429A=
ENST00000682805.1:n.4890A=
ENST00000682965.1:c.*692A= ENSP00000508229.1:n.*692A=
ENST00000683093.1:n.5569A=
ENST00000683136.1:c.4153A= ENSP00000507768.1:p.Ile1385=
ENST00000683153.1:n.4527A=
ENST00000683365.1:n.4587A=
ENST00000683377.1:n.4485A=
ENST00000683456.1:c.*1407A= ENSP00000508318.1:n.*1407A=
ENST00000683522.1:n.4485A=
ENST00000683562.1:c.*2439A= ENSP00000508265.1:n.*2439A=
ENST00000683693.1:n.6050A=
ENST00000683725.1:c.4270A= ENSP00000507496.1:p.Ile1424=
ENST00000684010.1:n.4480A=
ENST00000684157.1:n.5470A=
ENST00000684253.1:n.4388A=
ENST00000684288.1:c.*2442A= ENSP00000507143.1:n.*2442A=
ENST00000684313.1:n.3917A=
ENST00000684332.1:n.4558A=
ENST00000684371.1:n.4591A=
ENST00000684404.1:n.5513A=
ENST00000684442.1:n.4709A=
ENST00000684555.1:c.*2482A= ENSP00000507705.1:n.*2482A=
ENST00000684571.1:c.4111A= ENSP00000506935.1:p.Ile1371=
ENST00000684593.1:c.*3975A= ENSP00000507005.1:n.*3975A=
ENST00000684711.1:c.*2666A= ENSP00000506841.1:n.*2666A=
ENST00000302539.9:c.4273A= ENSP00000303960.4:p.Ile1425=
ENST00000389817.8:c.4270A= MANE Select ENSP00000374467.4:p.Ile1424=
ENST00000642271.1:c.4267A= ENSP00000493749.1:p.Ile1423=
ENST00000642579.1:c.2324A=
ENST00000642611.1:n.5488A=
ENST00000642902.1:c.4052A=
ENST00000643260.1:c.4270A= ENSP00000494450.1:p.Ile1424=
ENST00000643562.1:c.*2392A= ENSP00000496124.1:n.*2392A=
ENST00000643925.1:c.2910A=
ENST00000644057.1:n.347A=
ENST00000644484.1:c.*3656A= ENSP00000493558.1:n.*3656A=
ENST00000644675.1:c.*2442A= ENSP00000494567.1:n.*2442A=
ENST00000644757.1:c.*3202+617A= ENSP00000495085.1:n.*3202+617A=
ENST00000644772.1:c.4336A= ENSP00000494321.1:p.Ile1446=
ENST00000645004.1:n.1963A=
ENST00000645076.1:c.3469A=
ENST00000645417.1:c.1458A=
ENST00000645744.1:c.*3964-9A= ENSP00000494564.1:n.*3964-9A=
ENST00000645760.1:c.4691A=
ENST00000645884.1:c.*1553A= ENSP00000495516.1:n.*1553A=
ENST00000646003.1:c.*2301-9A= ENSP00000495259.1:n.*2301-9A=
ENST00000646207.1:c.*3107A= ENSP00000495025.1:n.*3107A=
ENST00000646276.1:c.*3674A= ENSP00000496070.1:n.*3674A=
ENST00000646592.1:c.3576A=
ENST00000646902.1:c.4237A= ENSP00000494101.1:p.Ile1413=
ENST00000646993.1:c.*2812A= ENSP00000493720.1:n.*2812A=
ENST00000647013.1:c.4276A= ENSP00000496741.1:n.4276A=
ENST00000647015.1:c.4021A= ENSP00000495389.1:p.Ile1341=
ENST00000647086.1:c.*3856A= ENSP00000493677.1:n.*3856A=
ENST00000647158.1:c.*2557A= ENSP00000495744.1:n.*2557A=
ENST00000302539.8:c.4273A= ENSP00000303960.4:p.Ile1425=
ENST00000389817.7:c.4270A= ENSP00000374467.3:p.Ile1424=
ENST00000525022.1:n.269A=
ENST00000526037.5:n.134A=
ENST00000526168.5:c.67-9A=
ENST00000531642.5:c.106A=
NM_000352.4:c.4270A= NP_000343.2:p.Ile1424=
NM_001287174.1:c.4273A= NP_001274103.1:p.Ile1425=
XM_011520331.1:c.4270A= XP_011518633.1:p.Ile1424=
XM_011520332.1:c.4273A= XP_011518634.1:p.Ile1425=
XM_011520333.1:c.2770A= XP_011518635.1:p.Ile924=
XR_930890.1:n.4336A=
NM_001351295.1:c.4336A= NP_001338224.1:p.Ile1446=
NM_001351296.1:c.4270A= NP_001338225.1:p.Ile1424=
NM_001351297.1:c.4267A= NP_001338226.1:p.Ile1423=
NR_147094.1:n.4565A=
XM_017018197.2:c.4339A= XP_016873686.1:p.Ile1447=
XM_017018199.1:c.4336A= XP_016873688.1:p.Ile1446=
XM_017018201.2:c.4339A= XP_016873690.1:p.Ile1447=
XM_017018202.1:c.2836A= XP_016873691.1:p.Ile946=
XM_017018204.1:c.2227A= XP_016873693.1:p.Ile743=
XM_024448668.1:c.2638A= XP_024304436.1:p.Ile880=
XR_001747945.2:n.4411A=
XR_001747946.2:n.4342A=
XR_002957189.1:n.6125A=
NM_000352.6:c.4270A= MANE Select NP_000343.2:p.Ile1424=
NM_001287174.2:c.4273A= NP_001274103.1:p.Ile1425=
NM_001351295.2:c.4336A= NP_001338224.1:p.Ile1446=
NM_001351296.2:c.4270A= NP_001338225.1:p.Ile1424=
NM_001351297.2:c.4267A= NP_001338226.1:p.Ile1423=
NR_147094.2:n.4565A=
NM_001287174.3:c.4273A= NP_001274103.1:p.Ile1425=