Canonical Allele Identifier: CA2612634568

Gene: ABCC8

Linked Data

• gnomAD v4: 11-17393243-GA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17393245del , CM000673.2:g.17393245del	GRCh38
NC_000011.9:g.17414792del , CM000673.1:g.17414792del	GRCh37
NC_000011.8:g.17371368del	NCBI36
NG_008867.1:g.88659del
NG_012446.1:g.416del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524561.2:n.4210-116del
ENST00000526037.6:n.544-116del
ENST00000528374.2:c.1200-116del
ENST00000529967.6:n.2948-116del
ENST00000532220.2:n.3842-116del
ENST00000642611.2:n.5942-116del
ENST00000644057.2:n.1185-116del
ENST00000645004.2:n.2108-116del
ENST00000682051.1:n.4771-116del
ENST00000682110.1:n.4824-116del
ENST00000682140.1:c.*395-116del	ENSP00000507829.1:n.*395-116del
ENST00000682185.1:n.5914-116del
ENST00000682204.1:c.*2747-116del	ENSP00000507094.1:n.*2747-116del
ENST00000682215.1:n.5191-116del
ENST00000682288.1:c.*3040-116del	ENSP00000507506.1:n.*3040-116del
ENST00000682442.1:n.5044-116del
ENST00000682528.1:n.4901-116del
ENST00000682673.1:n.4768-116del
ENST00000682805.1:n.5229-116del
ENST00000682965.1:c.*1031-116del	ENSP00000508229.1:n.*1031-116del
ENST00000683093.1:n.5804-116del
ENST00000683136.1:c.4492-116del	ENSP00000507768.1:n.4492-116del
ENST00000683153.1:n.4866-116del
ENST00000683365.1:n.4926-116del
ENST00000683377.1:n.4720-116del
ENST00000683456.1:c.*1746-116del	ENSP00000508318.1:n.*1746-116del
ENST00000683522.1:n.4906-116del
ENST00000683562.1:c.*2674-116del	ENSP00000508265.1:n.*2674-116del
ENST00000683693.1:n.6285-116del
ENST00000683725.1:c.*74-116del	ENSP00000507496.1:n.*74-116del
ENST00000684010.1:n.4819-116del
ENST00000684014.1:n.796-116del
ENST00000684157.1:n.5809-116del
ENST00000684253.1:n.4727-116del
ENST00000684288.1:c.*2781-116del	ENSP00000507143.1:n.*2781-116del
ENST00000684313.1:n.4256-116del
ENST00000684332.1:n.4897-116del
ENST00000684371.1:n.4930-116del
ENST00000684404.1:n.5852-116del
ENST00000684442.1:n.5048-116del
ENST00000684555.1:c.*2821-116del	ENSP00000507705.1:n.*2821-116del
ENST00000684571.1:c.4450-116del	ENSP00000506935.1:n.4450-116del
ENST00000684593.1:c.*4314-116del	ENSP00000507005.1:n.*4314-116del
ENST00000684711.1:c.*3005-116del	ENSP00000506841.1:n.*3005-116del
ENST00000302539.9:c.4612-116del	ENSP00000303960.4:n.4612-116del
ENST00000389817.8:c.4609-116del MANE Select	ENSP00000374467.4:n.4609-116del
ENST00000642271.1:c.4606-116del	ENSP00000493749.1:n.4606-116del
ENST00000642579.1:c.2663-116del
ENST00000642611.1:n.5827-116del
ENST00000642902.1:c.4391-116del
ENST00000643260.1:c.4609-116del	ENSP00000494450.1:n.4609-116del
ENST00000643562.1:c.*2731-116del	ENSP00000496124.1:n.*2731-116del
ENST00000643925.1:c.3186-116del
ENST00000644057.1:n.768-116del
ENST00000644484.1:c.*3995-116del	ENSP00000493558.1:n.*3995-116del
ENST00000644675.1:c.*2781-116del	ENSP00000494567.1:n.*2781-116del
ENST00000644757.1:c.*3203-264del	ENSP00000495085.1:n.*3203-264del
ENST00000644772.1:c.4675-116del	ENSP00000494321.1:n.4675-116del
ENST00000645004.1:n.2302-116del
ENST00000645076.1:c.3704-116del
ENST00000645417.1:c.1797-116del
ENST00000645744.1:c.*4294-116del	ENSP00000494564.1:n.*4294-116del
ENST00000645760.1:c.5030-116del
ENST00000645884.1:c.*1892-116del	ENSP00000495516.1:n.*1892-116del
ENST00000646003.1:c.*2631-116del	ENSP00000495259.1:n.*2631-116del
ENST00000646207.1:c.*3446-116del	ENSP00000495025.1:n.*3446-116del
ENST00000646276.1:c.*4013-116del	ENSP00000496070.1:n.*4013-116del
ENST00000646592.1:c.3915-116del
ENST00000646902.1:c.4576-116del	ENSP00000494101.1:n.4576-116del
ENST00000646993.1:c.*3047-116del	ENSP00000493720.1:n.*3047-116del
ENST00000647015.1:c.4360-116del	ENSP00000495389.1:n.4360-116del
ENST00000647086.1:c.*4195-116del	ENSP00000493677.1:n.*4195-116del
ENST00000647158.1:c.*2896-116del	ENSP00000495744.1:n.*2896-116del
ENST00000302539.8:c.4612-116del	ENSP00000303960.4:n.4612-116del
ENST00000389817.7:c.4609-116del	ENSP00000374467.3:n.4609-116del
ENST00000525022.1:n.504-32del
ENST00000526037.5:n.369-116del
ENST00000526168.5:c.397-116del
ENST00000531642.5:c.640-116del
NM_000352.4:c.4609-116del	NP_000343.2:n.4609-116del
NM_001287174.1:c.4612-116del	NP_001274103.1:n.4612-116del
XM_011520331.1:c.4609-116del	XP_011518633.1:n.4609-116del
XM_011520333.1:c.3109-116del	XP_011518635.1:n.3109-116del
XR_930890.1:n.4571-116del
NM_001351295.1:c.4675-116del	NP_001338224.1:n.4675-116del
NM_001351296.1:c.4609-116del	NP_001338225.1:n.4609-116del
NM_001351297.1:c.4606-116del	NP_001338226.1:n.4606-116del
NR_147094.1:n.4904-116del
XM_017018197.2:c.4678-116del	XP_016873686.1:n.4678-116del
XM_017018199.1:c.4675-116del	XP_016873688.1:n.4675-116del
XM_017018202.1:c.3175-116del	XP_016873691.1:n.3175-116del
XM_017018204.1:c.2566-116del	XP_016873693.1:n.2566-116del
XM_024448668.1:c.2977-116del	XP_024304436.1:n.2977-116del
XR_001747945.2:n.4646-116del
XR_001747946.2:n.4577-116del
XR_002957189.1:n.6360-116del
NM_000352.6:c.4609-116del MANE Select	NP_000343.2:n.4609-116del
NM_001287174.2:c.4612-116del	NP_001274103.1:n.4612-116del
NM_001351295.2:c.4675-116del	NP_001338224.1:n.4675-116del
NM_001351296.2:c.4609-116del	NP_001338225.1:n.4609-116del
NM_001351297.2:c.4606-116del	NP_001338226.1:n.4606-116del
NR_147094.2:n.4904-116del
NM_001287174.3:c.4612-116del	NP_001274103.1:n.4612-116del