Canonical Allele Identifier: CA2574768539

Gene: ABCC8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17397111C>A , CM000673.2:g.17397111C>A	GRCh38
NC_000011.9:g.17418658C>A , CM000673.1:g.17418658C>A	GRCh37
NC_000011.8:g.17375234C>A	NCBI36
NG_008867.1:g.84792G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524561.2:n.3525G>T
ENST00000528374.2:c.568-53G>T
ENST00000529967.6:n.2328-65G>T
ENST00000532220.2:n.2172G>T
ENST00000642611.2:n.4139G>T
ENST00000644057.2:n.432-65G>T
ENST00000645004.2:n.1488-65G>T
ENST00000682051.1:n.4086G>T
ENST00000682110.1:n.4139G>T
ENST00000682140.1:c.3985+82G>T	ENSP00000507829.1:n.3985+82G>T
ENST00000682185.1:n.5294-65G>T
ENST00000682204.1:c.*2127-65G>T	ENSP00000507094.1:n.*2127-65G>T
ENST00000682215.1:n.4506G>T
ENST00000682288.1:c.*2420-65G>T	ENSP00000507506.1:n.*2420-65G>T
ENST00000682442.1:n.4359G>T
ENST00000682528.1:n.4216G>T
ENST00000682673.1:n.4083G>T
ENST00000682805.1:n.4506G>T
ENST00000682965.1:c.*411-65G>T	ENSP00000508229.1:n.*411-65G>T
ENST00000683093.1:n.4238G>T
ENST00000683136.1:c.3872-65G>T	ENSP00000507768.1:n.3872-65G>T
ENST00000683153.1:n.4181G>T
ENST00000683365.1:n.4241G>T
ENST00000683377.1:n.4139G>T
ENST00000683456.1:c.*1126-65G>T	ENSP00000508318.1:n.*1126-65G>T
ENST00000683522.1:n.4139G>T
ENST00000683562.1:c.*2158-65G>T	ENSP00000508265.1:n.*2158-65G>T
ENST00000683693.1:n.4586G>T
ENST00000683725.1:c.3989-65G>T	ENSP00000507496.1:n.3989-65G>T
ENST00000684010.1:n.4134G>T
ENST00000684157.1:n.4139G>T
ENST00000684253.1:n.4042G>T
ENST00000684288.1:c.*2161-65G>T	ENSP00000507143.1:n.*2161-65G>T
ENST00000684313.1:n.3571G>T
ENST00000684332.1:n.4212G>T
ENST00000684371.1:n.4245G>T
ENST00000684404.1:n.4182G>T
ENST00000684442.1:n.4428-65G>T
ENST00000684555.1:c.*2201-65G>T	ENSP00000507705.1:n.*2201-65G>T
ENST00000684571.1:c.3830-65G>T	ENSP00000506935.1:n.3830-65G>T
ENST00000684593.1:c.*3694-65G>T	ENSP00000507005.1:n.*3694-65G>T
ENST00000684711.1:c.*2385-65G>T	ENSP00000506841.1:n.*2385-65G>T
ENST00000302539.9:c.3992-65G>T	ENSP00000303960.4:n.3992-65G>T
ENST00000389817.8:c.3989-65G>T MANE Select	ENSP00000374467.4:n.3989-65G>T
ENST00000642271.1:c.3986-65G>T	ENSP00000493749.1:n.3986-65G>T
ENST00000642579.1:c.2072+82G>T
ENST00000642611.1:n.4024G>T
ENST00000642902.1:c.3771-65G>T
ENST00000643260.1:c.3989-65G>T	ENSP00000494450.1:n.3989-65G>T
ENST00000643562.1:c.*2046G>T	ENSP00000496124.1:n.*2046G>T
ENST00000643925.1:c.2564G>T
ENST00000644057.1:n.1G>T
ENST00000644484.1:c.*2325G>T	ENSP00000493558.1:n.*2325G>T
ENST00000644675.1:c.*2161-65G>T	ENSP00000494567.1:n.*2161-65G>T
ENST00000644757.1:c.*2355G>T	ENSP00000495085.1:n.*2355G>T
ENST00000644772.1:c.4055-65G>T	ENSP00000494321.1:n.4055-65G>T
ENST00000645004.1:n.1579G>T
ENST00000645076.1:c.3188-65G>T
ENST00000645417.1:c.1177-65G>T
ENST00000645744.1:c.*2704G>T	ENSP00000494564.1:n.*2704G>T
ENST00000645760.1:c.4345G>T
ENST00000645884.1:c.*1207G>T	ENSP00000495516.1:n.*1207G>T
ENST00000646003.1:c.*2026G>T	ENSP00000495259.1:n.*2026G>T
ENST00000646207.1:c.*2826-65G>T	ENSP00000495025.1:n.*2826-65G>T
ENST00000646276.1:c.*2343G>T	ENSP00000496070.1:n.*2343G>T
ENST00000646592.1:c.3295-65G>T
ENST00000646902.1:c.3985+82G>T	ENSP00000494101.1:n.3985+82G>T
ENST00000646993.1:c.*2466G>T	ENSP00000493720.1:n.*2466G>T
ENST00000647013.1:c.3995-65G>T	ENSP00000496741.1:n.3995-65G>T
ENST00000647015.1:c.3740-65G>T	ENSP00000495389.1:n.3740-65G>T
ENST00000647086.1:c.*3604+82G>T	ENSP00000493677.1:n.*3604+82G>T
ENST00000647158.1:c.*2211G>T	ENSP00000495744.1:n.*2211G>T
ENST00000302539.8:c.3992-65G>T	ENSP00000303960.4:n.3992-65G>T
ENST00000389817.7:c.3989-65G>T	ENSP00000374467.3:n.3989-65G>T
ENST00000527905.5:c.*946G>T	ENSP00000431653.1:n.*946G>T
ENST00000528374.1:c.459-53G>T
ENST00000531137.1:n.489G>T
ENST00000531891.1:c.356+82G>T
ENST00000532220.1:n.398G>T
NM_000352.4:c.3989-65G>T	NP_000343.2:n.3989-65G>T
NM_001287174.1:c.3992-65G>T	NP_001274103.1:n.3992-65G>T
XM_011520331.1:c.3989-65G>T	XP_011518633.1:n.3989-65G>T
XM_011520332.1:c.3992-65G>T	XP_011518634.1:n.3992-65G>T
XM_011520333.1:c.2489-65G>T	XP_011518635.1:n.2489-65G>T
XR_930890.1:n.4055-65G>T
NM_001351295.1:c.4055-65G>T	NP_001338224.1:n.4055-65G>T
NM_001351296.1:c.3989-65G>T	NP_001338225.1:n.3989-65G>T
NM_001351297.1:c.3986-65G>T	NP_001338226.1:n.3986-65G>T
NR_147094.1:n.4219G>T
XM_017018197.2:c.4058-65G>T	XP_016873686.1:n.4058-65G>T
XM_017018199.1:c.4055-65G>T	XP_016873688.1:n.4055-65G>T
XM_017018201.2:c.4058-65G>T	XP_016873690.1:n.4058-65G>T
XM_017018202.1:c.2555-65G>T	XP_016873691.1:n.2555-65G>T
XM_017018204.1:c.1946-65G>T	XP_016873693.1:n.1946-65G>T
XM_024448668.1:c.2357-65G>T	XP_024304436.1:n.2357-65G>T
XR_001747945.2:n.4130-65G>T
XR_001747946.2:n.4061-65G>T
XR_002957189.1:n.4661G>T
NM_000352.6:c.3989-65G>T MANE Select	NP_000343.2:n.3989-65G>T
NM_001287174.2:c.3992-65G>T	NP_001274103.1:n.3992-65G>T
NM_001351295.2:c.4055-65G>T	NP_001338224.1:n.4055-65G>T
NM_001351296.2:c.3989-65G>T	NP_001338225.1:n.3989-65G>T
NM_001351297.2:c.3986-65G>T	NP_001338226.1:n.3986-65G>T
NR_147094.2:n.4219G>T
NM_001287174.3:c.3992-65G>T	NP_001274103.1:n.3992-65G>T