Canonical Allele Identifier: CA2739276235

Gene: ABCC8

Linked Data

• ClinVar Variation Id: 2853262
• ClinVar RCV Id: RCV003695942

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17393692del , CM000673.2:g.17393692del	GRCh38
NC_000011.9:g.17415239del , CM000673.1:g.17415239del	GRCh37
NC_000011.8:g.17371815del	NCBI36
NG_008867.1:g.88214del

Transcript Alleles

HGVS	Amino-acid change
ENST00000524561.2:n.4209+8del
ENST00000526037.6:n.543+8del
ENST00000528374.2:c.1199+8del
ENST00000529967.6:n.2947+8del
ENST00000532220.2:n.3841+8del
ENST00000642611.2:n.5941+8del
ENST00000644057.2:n.1184+8del
ENST00000645004.2:n.2107+8del
ENST00000682051.1:n.4770+8del
ENST00000682110.1:n.4823+8del
ENST00000682140.1:c.*394+8del	ENSP00000507829.1:n.*394+8del
ENST00000682185.1:n.5913+8del
ENST00000682204.1:c.*2746+8del	ENSP00000507094.1:n.*2746+8del
ENST00000682215.1:n.5190+8del
ENST00000682288.1:c.*3039+8del	ENSP00000507506.1:n.*3039+8del
ENST00000682442.1:n.5043+8del
ENST00000682528.1:n.4900+8del
ENST00000682673.1:n.4767+8del
ENST00000682805.1:n.5228+8del
ENST00000682965.1:c.*1030+8del	ENSP00000508229.1:n.*1030+8del
ENST00000683093.1:n.5803+8del
ENST00000683136.1:c.4491+8del	ENSP00000507768.1:n.4491+8del
ENST00000683153.1:n.4865+8del
ENST00000683365.1:n.4925+8del
ENST00000683377.1:n.4719+8del
ENST00000683456.1:c.*1745+8del	ENSP00000508318.1:n.*1745+8del
ENST00000683522.1:n.4905+8del
ENST00000683562.1:c.*2673+8del	ENSP00000508265.1:n.*2673+8del
ENST00000683693.1:n.6284+8del
ENST00000683725.1:c.*73+8del	ENSP00000507496.1:n.*73+8del
ENST00000684010.1:n.4818+8del
ENST00000684014.1:n.795+8del
ENST00000684157.1:n.5808+8del
ENST00000684253.1:n.4726+8del
ENST00000684288.1:c.*2780+8del	ENSP00000507143.1:n.*2780+8del
ENST00000684313.1:n.4255+8del
ENST00000684332.1:n.4896+8del
ENST00000684371.1:n.4929+8del
ENST00000684404.1:n.5851+8del
ENST00000684442.1:n.5047+8del
ENST00000684555.1:c.*2820+8del	ENSP00000507705.1:n.*2820+8del
ENST00000684571.1:c.4449+8del	ENSP00000506935.1:n.4449+8del
ENST00000684593.1:c.*4313+8del	ENSP00000507005.1:n.*4313+8del
ENST00000684711.1:c.*3004+8del	ENSP00000506841.1:n.*3004+8del
ENST00000302539.9:c.4611+8del	ENSP00000303960.4:n.4611+8del
ENST00000389817.8:c.4608+8del MANE Select	ENSP00000374467.4:n.4608+8del
ENST00000642271.1:c.4605+8del	ENSP00000493749.1:n.4605+8del
ENST00000642579.1:c.2662+8del
ENST00000642611.1:n.5826+8del
ENST00000642902.1:c.4390+8del
ENST00000643260.1:c.4608+8del	ENSP00000494450.1:n.4608+8del
ENST00000643562.1:c.*2730+8del	ENSP00000496124.1:n.*2730+8del
ENST00000643925.1:c.3186-561del
ENST00000644057.1:n.767+8del
ENST00000644484.1:c.*3994+8del	ENSP00000493558.1:n.*3994+8del
ENST00000644675.1:c.*2780+8del	ENSP00000494567.1:n.*2780+8del
ENST00000644757.1:c.*3203-709del	ENSP00000495085.1:n.*3203-709del
ENST00000644772.1:c.4674+8del	ENSP00000494321.1:n.4674+8del
ENST00000645004.1:n.2301+8del
ENST00000645076.1:c.3703+8del
ENST00000645417.1:c.1796+8del
ENST00000645744.1:c.*4293+8del	ENSP00000494564.1:n.*4293+8del
ENST00000645760.1:c.5029+8del
ENST00000645884.1:c.*1891+8del	ENSP00000495516.1:n.*1891+8del
ENST00000646003.1:c.*2630+8del	ENSP00000495259.1:n.*2630+8del
ENST00000646207.1:c.*3445+8del	ENSP00000495025.1:n.*3445+8del
ENST00000646276.1:c.*4012+8del	ENSP00000496070.1:n.*4012+8del
ENST00000646592.1:c.3914+8del
ENST00000646902.1:c.4575+8del	ENSP00000494101.1:n.4575+8del
ENST00000646993.1:c.*3046+8del	ENSP00000493720.1:n.*3046+8del
ENST00000647015.1:c.4359+8del	ENSP00000495389.1:n.4359+8del
ENST00000647086.1:c.*4194+8del	ENSP00000493677.1:n.*4194+8del
ENST00000647158.1:c.*2895+8del	ENSP00000495744.1:n.*2895+8del
ENST00000302539.8:c.4611+8del	ENSP00000303960.4:n.4611+8del
ENST00000389817.7:c.4608+8del	ENSP00000374467.3:n.4608+8del
ENST00000525022.1:n.503+8del
ENST00000526037.5:n.368+8del
ENST00000526168.5:c.396+8del
ENST00000531642.5:c.639+8del
NM_000352.4:c.4608+8del	NP_000343.2:n.4608+8del
NM_001287174.1:c.4611+8del	NP_001274103.1:n.4611+8del
XM_011520331.1:c.4608+8del	XP_011518633.1:n.4608+8del
XM_011520333.1:c.3108+8del	XP_011518635.1:n.3108+8del
XR_930890.1:n.4570+8del
NM_001351295.1:c.4674+8del	NP_001338224.1:n.4674+8del
NM_001351296.1:c.4608+8del	NP_001338225.1:n.4608+8del
NM_001351297.1:c.4605+8del	NP_001338226.1:n.4605+8del
NR_147094.1:n.4903+8del
XM_017018197.2:c.4677+8del	XP_016873686.1:n.4677+8del
XM_017018199.1:c.4674+8del	XP_016873688.1:n.4674+8del
XM_017018202.1:c.3174+8del	XP_016873691.1:n.3174+8del
XM_017018204.1:c.2565+8del	XP_016873693.1:n.2565+8del
XM_024448668.1:c.2976+8del	XP_024304436.1:n.2976+8del
XR_001747945.2:n.4645+8del
XR_001747946.2:n.4576+8del
XR_002957189.1:n.6359+8del
NM_000352.6:c.4608+8del MANE Select	NP_000343.2:n.4608+8del
NM_001287174.2:c.4611+8del	NP_001274103.1:n.4611+8del
NM_001351295.2:c.4674+8del	NP_001338224.1:n.4674+8del
NM_001351296.2:c.4608+8del	NP_001338225.1:n.4608+8del
NM_001351297.2:c.4605+8del	NP_001338226.1:n.4605+8del
NR_147094.2:n.4903+8del
NM_001287174.3:c.4611+8del	NP_001274103.1:n.4611+8del