Canonical Allele Identifier: CA1955123938

Gene: ABCC8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17397012T= , CM000673.2:g.17397012T=	GRCh38
NC_000011.9:g.17418559T= , CM000673.1:g.17418559T=	GRCh37
NC_000011.8:g.17375135T=	NCBI36
NG_008867.1:g.84891A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524561.2:n.3624A=
ENST00000528374.2:c.614A=
ENST00000529967.6:n.2362A=
ENST00000532220.2:n.2271A=
ENST00000642611.2:n.4238A=
ENST00000644057.2:n.466A=
ENST00000645004.2:n.1522A=
ENST00000682051.1:n.4185A=
ENST00000682110.1:n.4238A=
ENST00000682140.1:c.3985+181A=	ENSP00000507829.1:n.3985+181A=
ENST00000682185.1:n.5328A=
ENST00000682204.1:c.*2161A=	ENSP00000507094.1:n.*2161A=
ENST00000682215.1:n.4605A=
ENST00000682288.1:c.*2454A=	ENSP00000507506.1:n.*2454A=
ENST00000682442.1:n.4458A=
ENST00000682528.1:n.4315A=
ENST00000682673.1:n.4182A=
ENST00000682805.1:n.4605A=
ENST00000682965.1:c.*445A=	ENSP00000508229.1:n.*445A=
ENST00000683093.1:n.4337A=
ENST00000683136.1:c.3906A=	ENSP00000507768.1:p.Gln1302=
ENST00000683153.1:n.4280A=
ENST00000683365.1:n.4340A=
ENST00000683377.1:n.4238A=
ENST00000683456.1:c.*1160A=	ENSP00000508318.1:n.*1160A=
ENST00000683522.1:n.4238A=
ENST00000683562.1:c.*2192A=	ENSP00000508265.1:n.*2192A=
ENST00000683693.1:n.4685A=
ENST00000683725.1:c.4023A=	ENSP00000507496.1:p.Gln1341=
ENST00000684010.1:n.4233A=
ENST00000684157.1:n.4238A=
ENST00000684253.1:n.4141A=
ENST00000684288.1:c.*2195A=	ENSP00000507143.1:n.*2195A=
ENST00000684313.1:n.3670A=
ENST00000684332.1:n.4311A=
ENST00000684371.1:n.4344A=
ENST00000684404.1:n.4281A=
ENST00000684442.1:n.4462A=
ENST00000684555.1:c.*2235A=	ENSP00000507705.1:n.*2235A=
ENST00000684571.1:c.3864A=	ENSP00000506935.1:p.Gln1288=
ENST00000684593.1:c.*3728A=	ENSP00000507005.1:n.*3728A=
ENST00000684711.1:c.*2419A=	ENSP00000506841.1:n.*2419A=
ENST00000302539.9:c.4026A=	ENSP00000303960.4:p.Gln1342=
ENST00000389817.8:c.4023A= MANE Select	ENSP00000374467.4:p.Gln1341=
ENST00000642271.1:c.4020A=	ENSP00000493749.1:p.Gln1340=
ENST00000642579.1:c.2077A=
ENST00000642611.1:n.4123A=
ENST00000642902.1:c.3805A=
ENST00000643260.1:c.4023A=	ENSP00000494450.1:p.Gln1341=
ENST00000643562.1:c.*2145A=	ENSP00000496124.1:n.*2145A=
ENST00000643925.1:c.2663A=
ENST00000644057.1:n.100A=
ENST00000644484.1:c.*2424A=	ENSP00000493558.1:n.*2424A=
ENST00000644675.1:c.*2195A=	ENSP00000494567.1:n.*2195A=
ENST00000644757.1:c.*2454A=	ENSP00000495085.1:n.*2454A=
ENST00000644772.1:c.4089A=	ENSP00000494321.1:p.Gln1363=
ENST00000645004.1:n.1678A=
ENST00000645076.1:c.3222A=
ENST00000645417.1:c.1211A=
ENST00000645744.1:c.*2803A=	ENSP00000494564.1:n.*2803A=
ENST00000645760.1:c.4444A=
ENST00000645884.1:c.*1306A=	ENSP00000495516.1:n.*1306A=
ENST00000646003.1:c.*2125A=	ENSP00000495259.1:n.*2125A=
ENST00000646207.1:c.*2860A=	ENSP00000495025.1:n.*2860A=
ENST00000646276.1:c.*2442A=	ENSP00000496070.1:n.*2442A=
ENST00000646592.1:c.3329A=
ENST00000646902.1:c.3990A=	ENSP00000494101.1:p.Gln1330=
ENST00000646993.1:c.*2565A=	ENSP00000493720.1:n.*2565A=
ENST00000647013.1:c.4029A=	ENSP00000496741.1:n.4029A=
ENST00000647015.1:c.3774A=	ENSP00000495389.1:p.Gln1258=
ENST00000647086.1:c.*3609A=	ENSP00000493677.1:n.*3609A=
ENST00000647158.1:c.*2310A=	ENSP00000495744.1:n.*2310A=
ENST00000302539.8:c.4026A=	ENSP00000303960.4:p.Gln1342=
ENST00000389817.7:c.4023A=	ENSP00000374467.3:p.Gln1341=
ENST00000527905.5:c.*1045A=	ENSP00000431653.1:n.*1045A=
ENST00000528374.1:c.505A=
ENST00000531137.1:n.588A=
ENST00000531891.1:c.361A=
ENST00000532220.1:n.497A=
NM_000352.4:c.4023A=	NP_000343.2:p.Gln1341=
NM_001287174.1:c.4026A=	NP_001274103.1:p.Gln1342=
XM_011520331.1:c.4023A=	XP_011518633.1:p.Gln1341=
XM_011520332.1:c.4026A=	XP_011518634.1:p.Gln1342=
XM_011520333.1:c.2523A=	XP_011518635.1:p.Gln841=
XR_930890.1:n.4089A=
NM_001351295.1:c.4089A=	NP_001338224.1:p.Gln1363=
NM_001351296.1:c.4023A=	NP_001338225.1:p.Gln1341=
NM_001351297.1:c.4020A=	NP_001338226.1:p.Gln1340=
NR_147094.1:n.4318A=
XM_017018197.2:c.4092A=	XP_016873686.1:p.Gln1364=
XM_017018199.1:c.4089A=	XP_016873688.1:p.Gln1363=
XM_017018201.2:c.4092A=	XP_016873690.1:p.Gln1364=
XM_017018202.1:c.2589A=	XP_016873691.1:p.Gln863=
XM_017018204.1:c.1980A=	XP_016873693.1:p.Gln660=
XM_024448668.1:c.2391A=	XP_024304436.1:p.Gln797=
XR_001747945.2:n.4164A=
XR_001747946.2:n.4095A=
XR_002957189.1:n.4760A=
NM_000352.6:c.4023A= MANE Select	NP_000343.2:p.Gln1341=
NM_001287174.2:c.4026A=	NP_001274103.1:p.Gln1342=
NM_001351295.2:c.4089A=	NP_001338224.1:p.Gln1363=
NM_001351296.2:c.4023A=	NP_001338225.1:p.Gln1341=
NM_001351297.2:c.4020A=	NP_001338226.1:p.Gln1340=
NR_147094.2:n.4318A=
NM_001287174.3:c.4026A=	NP_001274103.1:p.Gln1342=