Canonical Allele Identifier: CA1955123928

Gene: ABCC8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17396992T= , CM000673.2:g.17396992T=	GRCh38
NC_000011.9:g.17418539T= , CM000673.1:g.17418539T=	GRCh37
NC_000011.8:g.17375115T=	NCBI36
NG_008867.1:g.84911A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524561.2:n.3644A=
ENST00000528374.2:c.634A=
ENST00000529967.6:n.2382A=
ENST00000532220.2:n.2291A=
ENST00000642611.2:n.4258A=
ENST00000644057.2:n.486A=
ENST00000645004.2:n.1542A=
ENST00000682051.1:n.4205A=
ENST00000682110.1:n.4258A=
ENST00000682140.1:c.3985+201A=	ENSP00000507829.1:n.3985+201A=
ENST00000682185.1:n.5348A=
ENST00000682204.1:c.*2181A=	ENSP00000507094.1:n.*2181A=
ENST00000682215.1:n.4625A=
ENST00000682288.1:c.*2474A=	ENSP00000507506.1:n.*2474A=
ENST00000682442.1:n.4478A=
ENST00000682528.1:n.4335A=
ENST00000682673.1:n.4202A=
ENST00000682805.1:n.4625A=
ENST00000682965.1:c.*465A=	ENSP00000508229.1:n.*465A=
ENST00000683093.1:n.4357A=
ENST00000683136.1:c.3926A=	ENSP00000507768.1:p.Asn1309=
ENST00000683153.1:n.4300A=
ENST00000683365.1:n.4360A=
ENST00000683377.1:n.4258A=
ENST00000683456.1:c.*1180A=	ENSP00000508318.1:n.*1180A=
ENST00000683522.1:n.4258A=
ENST00000683562.1:c.*2212A=	ENSP00000508265.1:n.*2212A=
ENST00000683693.1:n.4705A=
ENST00000683725.1:c.4043A=	ENSP00000507496.1:p.Asn1348=
ENST00000684010.1:n.4253A=
ENST00000684157.1:n.4258A=
ENST00000684253.1:n.4161A=
ENST00000684288.1:c.*2215A=	ENSP00000507143.1:n.*2215A=
ENST00000684313.1:n.3690A=
ENST00000684332.1:n.4331A=
ENST00000684371.1:n.4364A=
ENST00000684404.1:n.4301A=
ENST00000684442.1:n.4482A=
ENST00000684555.1:c.*2255A=	ENSP00000507705.1:n.*2255A=
ENST00000684571.1:c.3884A=	ENSP00000506935.1:p.Asn1295=
ENST00000684593.1:c.*3748A=	ENSP00000507005.1:n.*3748A=
ENST00000684711.1:c.*2439A=	ENSP00000506841.1:n.*2439A=
ENST00000302539.9:c.4046A=	ENSP00000303960.4:p.Asn1349=
ENST00000389817.8:c.4043A= MANE Select	ENSP00000374467.4:p.Asn1348=
ENST00000642271.1:c.4040A=	ENSP00000493749.1:p.Asn1347=
ENST00000642579.1:c.2097A=
ENST00000642611.1:n.4143A=
ENST00000642902.1:c.3825A=
ENST00000643260.1:c.4043A=	ENSP00000494450.1:p.Asn1348=
ENST00000643562.1:c.*2165A=	ENSP00000496124.1:n.*2165A=
ENST00000643925.1:c.2683A=
ENST00000644057.1:n.120A=
ENST00000644484.1:c.*2444A=	ENSP00000493558.1:n.*2444A=
ENST00000644675.1:c.*2215A=	ENSP00000494567.1:n.*2215A=
ENST00000644757.1:c.*2474A=	ENSP00000495085.1:n.*2474A=
ENST00000644772.1:c.4109A=	ENSP00000494321.1:p.Asn1370=
ENST00000645004.1:n.1698A=
ENST00000645076.1:c.3242A=
ENST00000645417.1:c.1231A=
ENST00000645744.1:c.*2823A=	ENSP00000494564.1:n.*2823A=
ENST00000645760.1:c.4464A=
ENST00000645884.1:c.*1326A=	ENSP00000495516.1:n.*1326A=
ENST00000646003.1:c.*2145A=	ENSP00000495259.1:n.*2145A=
ENST00000646207.1:c.*2880A=	ENSP00000495025.1:n.*2880A=
ENST00000646276.1:c.*2462A=	ENSP00000496070.1:n.*2462A=
ENST00000646592.1:c.3349A=
ENST00000646902.1:c.4010A=	ENSP00000494101.1:p.Asn1337=
ENST00000646993.1:c.*2585A=	ENSP00000493720.1:n.*2585A=
ENST00000647013.1:c.4049A=	ENSP00000496741.1:n.4049A=
ENST00000647015.1:c.3794A=	ENSP00000495389.1:p.Asn1265=
ENST00000647086.1:c.*3629A=	ENSP00000493677.1:n.*3629A=
ENST00000647158.1:c.*2330A=	ENSP00000495744.1:n.*2330A=
ENST00000302539.8:c.4046A=	ENSP00000303960.4:p.Asn1349=
ENST00000389817.7:c.4043A=	ENSP00000374467.3:p.Asn1348=
ENST00000527905.5:c.*1065A=	ENSP00000431653.1:n.*1065A=
ENST00000528374.1:c.525A=
ENST00000531137.1:n.608A=
ENST00000531891.1:c.381A=
ENST00000532220.1:n.517A=
NM_000352.4:c.4043A=	NP_000343.2:p.Asn1348=
NM_001287174.1:c.4046A=	NP_001274103.1:p.Asn1349=
XM_011520331.1:c.4043A=	XP_011518633.1:p.Asn1348=
XM_011520332.1:c.4046A=	XP_011518634.1:p.Asn1349=
XM_011520333.1:c.2543A=	XP_011518635.1:p.Asn848=
XR_930890.1:n.4109A=
NM_001351295.1:c.4109A=	NP_001338224.1:p.Asn1370=
NM_001351296.1:c.4043A=	NP_001338225.1:p.Asn1348=
NM_001351297.1:c.4040A=	NP_001338226.1:p.Asn1347=
NR_147094.1:n.4338A=
XM_017018197.2:c.4112A=	XP_016873686.1:p.Asn1371=
XM_017018199.1:c.4109A=	XP_016873688.1:p.Asn1370=
XM_017018201.2:c.4112A=	XP_016873690.1:p.Asn1371=
XM_017018202.1:c.2609A=	XP_016873691.1:p.Asn870=
XM_017018204.1:c.2000A=	XP_016873693.1:p.Asn667=
XM_024448668.1:c.2411A=	XP_024304436.1:p.Asn804=
XR_001747945.2:n.4184A=
XR_001747946.2:n.4115A=
XR_002957189.1:n.4780A=
NM_000352.6:c.4043A= MANE Select	NP_000343.2:p.Asn1348=
NM_001287174.2:c.4046A=	NP_001274103.1:p.Asn1349=
NM_001351295.2:c.4109A=	NP_001338224.1:p.Asn1370=
NM_001351296.2:c.4043A=	NP_001338225.1:p.Asn1348=
NM_001351297.2:c.4040A=	NP_001338226.1:p.Asn1347=
NR_147094.2:n.4338A=
NM_001287174.3:c.4046A=	NP_001274103.1:p.Asn1349=