Canonical Allele Identifier: CA2612634994

Gene: ABCC8

Linked Data

• gnomAD v4: 11-17393355-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17393355C>A , CM000673.2:g.17393355C>A	GRCh38
NC_000011.9:g.17414902C>A , CM000673.1:g.17414902C>A	GRCh37
NC_000011.8:g.17371478C>A	NCBI36
NG_008867.1:g.88548G>T
NG_012446.1:g.305G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524561.2:n.4210-227G>T
ENST00000526037.6:n.544-227G>T
ENST00000528374.2:c.1200-227G>T
ENST00000529967.6:n.2948-227G>T
ENST00000532220.2:n.3842-227G>T
ENST00000642611.2:n.5942-227G>T
ENST00000644057.2:n.1185-227G>T
ENST00000645004.2:n.2108-227G>T
ENST00000682051.1:n.4771-227G>T
ENST00000682110.1:n.4824-227G>T
ENST00000682140.1:c.*395-227G>T	ENSP00000507829.1:n.*395-227G>T
ENST00000682185.1:n.5914-227G>T
ENST00000682204.1:c.*2747-227G>T	ENSP00000507094.1:n.*2747-227G>T
ENST00000682215.1:n.5191-227G>T
ENST00000682288.1:c.*3040-227G>T	ENSP00000507506.1:n.*3040-227G>T
ENST00000682442.1:n.5044-227G>T
ENST00000682528.1:n.4901-227G>T
ENST00000682673.1:n.4768-227G>T
ENST00000682805.1:n.5229-227G>T
ENST00000682965.1:c.*1031-227G>T	ENSP00000508229.1:n.*1031-227G>T
ENST00000683093.1:n.5804-227G>T
ENST00000683136.1:c.4492-227G>T	ENSP00000507768.1:n.4492-227G>T
ENST00000683153.1:n.4866-227G>T
ENST00000683365.1:n.4926-227G>T
ENST00000683377.1:n.4720-227G>T
ENST00000683456.1:c.*1746-227G>T	ENSP00000508318.1:n.*1746-227G>T
ENST00000683522.1:n.4906-227G>T
ENST00000683562.1:c.*2674-227G>T	ENSP00000508265.1:n.*2674-227G>T
ENST00000683693.1:n.6285-227G>T
ENST00000683725.1:c.*74-227G>T	ENSP00000507496.1:n.*74-227G>T
ENST00000684010.1:n.4819-227G>T
ENST00000684014.1:n.796-227G>T
ENST00000684157.1:n.5809-227G>T
ENST00000684253.1:n.4727-227G>T
ENST00000684288.1:c.*2781-227G>T	ENSP00000507143.1:n.*2781-227G>T
ENST00000684313.1:n.4256-227G>T
ENST00000684332.1:n.4897-227G>T
ENST00000684371.1:n.4930-227G>T
ENST00000684404.1:n.5852-227G>T
ENST00000684442.1:n.5048-227G>T
ENST00000684555.1:c.*2821-227G>T	ENSP00000507705.1:n.*2821-227G>T
ENST00000684571.1:c.4450-227G>T	ENSP00000506935.1:n.4450-227G>T
ENST00000684593.1:c.*4314-227G>T	ENSP00000507005.1:n.*4314-227G>T
ENST00000684711.1:c.*3005-227G>T	ENSP00000506841.1:n.*3005-227G>T
ENST00000302539.9:c.4612-227G>T	ENSP00000303960.4:n.4612-227G>T
ENST00000389817.8:c.4609-227G>T MANE Select	ENSP00000374467.4:n.4609-227G>T
ENST00000642271.1:c.4606-227G>T	ENSP00000493749.1:n.4606-227G>T
ENST00000642579.1:c.2663-227G>T
ENST00000642611.1:n.5827-227G>T
ENST00000642902.1:c.4391-227G>T
ENST00000643260.1:c.4609-227G>T	ENSP00000494450.1:n.4609-227G>T
ENST00000643562.1:c.*2731-227G>T	ENSP00000496124.1:n.*2731-227G>T
ENST00000643925.1:c.3186-227G>T
ENST00000644057.1:n.768-227G>T
ENST00000644484.1:c.*3995-227G>T	ENSP00000493558.1:n.*3995-227G>T
ENST00000644675.1:c.*2781-227G>T	ENSP00000494567.1:n.*2781-227G>T
ENST00000644757.1:c.*3203-375G>T	ENSP00000495085.1:n.*3203-375G>T
ENST00000644772.1:c.4675-227G>T	ENSP00000494321.1:n.4675-227G>T
ENST00000645004.1:n.2302-227G>T
ENST00000645076.1:c.3704-227G>T
ENST00000645417.1:c.1797-227G>T
ENST00000645744.1:c.*4294-227G>T	ENSP00000494564.1:n.*4294-227G>T
ENST00000645760.1:c.5030-227G>T
ENST00000645884.1:c.*1892-227G>T	ENSP00000495516.1:n.*1892-227G>T
ENST00000646003.1:c.*2631-227G>T	ENSP00000495259.1:n.*2631-227G>T
ENST00000646207.1:c.*3446-227G>T	ENSP00000495025.1:n.*3446-227G>T
ENST00000646276.1:c.*4013-227G>T	ENSP00000496070.1:n.*4013-227G>T
ENST00000646592.1:c.3915-227G>T
ENST00000646902.1:c.4576-227G>T	ENSP00000494101.1:n.4576-227G>T
ENST00000646993.1:c.*3047-227G>T	ENSP00000493720.1:n.*3047-227G>T
ENST00000647015.1:c.4360-227G>T	ENSP00000495389.1:n.4360-227G>T
ENST00000647086.1:c.*4195-227G>T	ENSP00000493677.1:n.*4195-227G>T
ENST00000647158.1:c.*2896-227G>T	ENSP00000495744.1:n.*2896-227G>T
ENST00000302539.8:c.4612-227G>T	ENSP00000303960.4:n.4612-227G>T
ENST00000389817.7:c.4609-227G>T	ENSP00000374467.3:n.4609-227G>T
ENST00000525022.1:n.504-143G>T
ENST00000526037.5:n.369-227G>T
ENST00000526168.5:c.397-227G>T
ENST00000531642.5:c.640-227G>T
NM_000352.4:c.4609-227G>T	NP_000343.2:n.4609-227G>T
NM_001287174.1:c.4612-227G>T	NP_001274103.1:n.4612-227G>T
XM_011520331.1:c.4609-227G>T	XP_011518633.1:n.4609-227G>T
XM_011520333.1:c.3109-227G>T	XP_011518635.1:n.3109-227G>T
XR_930890.1:n.4571-227G>T
NM_001351295.1:c.4675-227G>T	NP_001338224.1:n.4675-227G>T
NM_001351296.1:c.4609-227G>T	NP_001338225.1:n.4609-227G>T
NM_001351297.1:c.4606-227G>T	NP_001338226.1:n.4606-227G>T
NR_147094.1:n.4904-227G>T
XM_017018197.2:c.4678-227G>T	XP_016873686.1:n.4678-227G>T
XM_017018199.1:c.4675-227G>T	XP_016873688.1:n.4675-227G>T
XM_017018202.1:c.3175-227G>T	XP_016873691.1:n.3175-227G>T
XM_017018204.1:c.2566-227G>T	XP_016873693.1:n.2566-227G>T
XM_024448668.1:c.2977-227G>T	XP_024304436.1:n.2977-227G>T
XR_001747945.2:n.4646-227G>T
XR_001747946.2:n.4577-227G>T
XR_002957189.1:n.6360-227G>T
NM_000352.6:c.4609-227G>T MANE Select	NP_000343.2:n.4609-227G>T
NM_001287174.2:c.4612-227G>T	NP_001274103.1:n.4612-227G>T
NM_001351295.2:c.4675-227G>T	NP_001338224.1:n.4675-227G>T
NM_001351296.2:c.4609-227G>T	NP_001338225.1:n.4609-227G>T
NM_001351297.2:c.4606-227G>T	NP_001338226.1:n.4606-227G>T
NR_147094.2:n.4904-227G>T
NM_001287174.3:c.4612-227G>T	NP_001274103.1:n.4612-227G>T