Canonical Allele Identifier: CA1955123942

Gene: ABCC8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17397019G= , CM000673.2:g.17397019G=	GRCh38
NC_000011.9:g.17418566G= , CM000673.1:g.17418566G=	GRCh37
NC_000011.8:g.17375142G=	NCBI36
NG_008867.1:g.84884C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524561.2:n.3617C=
ENST00000528374.2:c.607C=
ENST00000529967.6:n.2355C=
ENST00000532220.2:n.2264C=
ENST00000642611.2:n.4231C=
ENST00000644057.2:n.459C=
ENST00000645004.2:n.1515C=
ENST00000682051.1:n.4178C=
ENST00000682110.1:n.4231C=
ENST00000682140.1:c.3985+174C=	ENSP00000507829.1:n.3985+174C=
ENST00000682185.1:n.5321C=
ENST00000682204.1:c.*2154C=	ENSP00000507094.1:n.*2154C=
ENST00000682215.1:n.4598C=
ENST00000682288.1:c.*2447C=	ENSP00000507506.1:n.*2447C=
ENST00000682442.1:n.4451C=
ENST00000682528.1:n.4308C=
ENST00000682673.1:n.4175C=
ENST00000682805.1:n.4598C=
ENST00000682965.1:c.*438C=	ENSP00000508229.1:n.*438C=
ENST00000683093.1:n.4330C=
ENST00000683136.1:c.3899C=	ENSP00000507768.1:p.Pro1300=
ENST00000683153.1:n.4273C=
ENST00000683365.1:n.4333C=
ENST00000683377.1:n.4231C=
ENST00000683456.1:c.*1153C=	ENSP00000508318.1:n.*1153C=
ENST00000683522.1:n.4231C=
ENST00000683562.1:c.*2185C=	ENSP00000508265.1:n.*2185C=
ENST00000683693.1:n.4678C=
ENST00000683725.1:c.4016C=	ENSP00000507496.1:p.Pro1339=
ENST00000684010.1:n.4226C=
ENST00000684157.1:n.4231C=
ENST00000684253.1:n.4134C=
ENST00000684288.1:c.*2188C=	ENSP00000507143.1:n.*2188C=
ENST00000684313.1:n.3663C=
ENST00000684332.1:n.4304C=
ENST00000684371.1:n.4337C=
ENST00000684404.1:n.4274C=
ENST00000684442.1:n.4455C=
ENST00000684555.1:c.*2228C=	ENSP00000507705.1:n.*2228C=
ENST00000684571.1:c.3857C=	ENSP00000506935.1:p.Pro1286=
ENST00000684593.1:c.*3721C=	ENSP00000507005.1:n.*3721C=
ENST00000684711.1:c.*2412C=	ENSP00000506841.1:n.*2412C=
ENST00000302539.9:c.4019C=	ENSP00000303960.4:p.Pro1340=
ENST00000389817.8:c.4016C= MANE Select	ENSP00000374467.4:p.Pro1339=
ENST00000642271.1:c.4013C=	ENSP00000493749.1:p.Pro1338=
ENST00000642579.1:c.2073-3C=
ENST00000642611.1:n.4116C=
ENST00000642902.1:c.3798C=
ENST00000643260.1:c.4016C=	ENSP00000494450.1:p.Pro1339=
ENST00000643562.1:c.*2138C=	ENSP00000496124.1:n.*2138C=
ENST00000643925.1:c.2656C=
ENST00000644057.1:n.93C=
ENST00000644484.1:c.*2417C=	ENSP00000493558.1:n.*2417C=
ENST00000644675.1:c.*2188C=	ENSP00000494567.1:n.*2188C=
ENST00000644757.1:c.*2447C=	ENSP00000495085.1:n.*2447C=
ENST00000644772.1:c.4082C=	ENSP00000494321.1:p.Pro1361=
ENST00000645004.1:n.1671C=
ENST00000645076.1:c.3215C=
ENST00000645417.1:c.1204C=
ENST00000645744.1:c.*2796C=	ENSP00000494564.1:n.*2796C=
ENST00000645760.1:c.4437C=
ENST00000645884.1:c.*1299C=	ENSP00000495516.1:n.*1299C=
ENST00000646003.1:c.*2118C=	ENSP00000495259.1:n.*2118C=
ENST00000646207.1:c.*2853C=	ENSP00000495025.1:n.*2853C=
ENST00000646276.1:c.*2435C=	ENSP00000496070.1:n.*2435C=
ENST00000646592.1:c.3322C=
ENST00000646902.1:c.3986-3C=	ENSP00000494101.1:n.3986-3C=
ENST00000646993.1:c.*2558C=	ENSP00000493720.1:n.*2558C=
ENST00000647013.1:c.4022C=	ENSP00000496741.1:n.4022C=
ENST00000647015.1:c.3767C=	ENSP00000495389.1:p.Pro1256=
ENST00000647086.1:c.*3605-3C=	ENSP00000493677.1:n.*3605-3C=
ENST00000647158.1:c.*2303C=	ENSP00000495744.1:n.*2303C=
ENST00000302539.8:c.4019C=	ENSP00000303960.4:p.Pro1340=
ENST00000389817.7:c.4016C=	ENSP00000374467.3:p.Pro1339=
ENST00000527905.5:c.*1038C=	ENSP00000431653.1:n.*1038C=
ENST00000528374.1:c.498C=
ENST00000531137.1:n.581C=
ENST00000531891.1:c.357-3C=
ENST00000532220.1:n.490C=
NM_000352.4:c.4016C=	NP_000343.2:p.Pro1339=
NM_001287174.1:c.4019C=	NP_001274103.1:p.Pro1340=
XM_011520331.1:c.4016C=	XP_011518633.1:p.Pro1339=
XM_011520332.1:c.4019C=	XP_011518634.1:p.Pro1340=
XM_011520333.1:c.2516C=	XP_011518635.1:p.Pro839=
XR_930890.1:n.4082C=
NM_001351295.1:c.4082C=	NP_001338224.1:p.Pro1361=
NM_001351296.1:c.4016C=	NP_001338225.1:p.Pro1339=
NM_001351297.1:c.4013C=	NP_001338226.1:p.Pro1338=
NR_147094.1:n.4311C=
XM_017018197.2:c.4085C=	XP_016873686.1:p.Pro1362=
XM_017018199.1:c.4082C=	XP_016873688.1:p.Pro1361=
XM_017018201.2:c.4085C=	XP_016873690.1:p.Pro1362=
XM_017018202.1:c.2582C=	XP_016873691.1:p.Pro861=
XM_017018204.1:c.1973C=	XP_016873693.1:p.Pro658=
XM_024448668.1:c.2384C=	XP_024304436.1:p.Pro795=
XR_001747945.2:n.4157C=
XR_001747946.2:n.4088C=
XR_002957189.1:n.4753C=
NM_000352.6:c.4016C= MANE Select	NP_000343.2:p.Pro1339=
NM_001287174.2:c.4019C=	NP_001274103.1:p.Pro1340=
NM_001351295.2:c.4082C=	NP_001338224.1:p.Pro1361=
NM_001351296.2:c.4016C=	NP_001338225.1:p.Pro1339=
NM_001351297.2:c.4013C=	NP_001338226.1:p.Pro1338=
NR_147094.2:n.4311C=
NM_001287174.3:c.4019C=	NP_001274103.1:p.Pro1340=