Canonical Allele Identifier: CA1955122309

Gene: ABCC8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17393742C= , CM000673.2:g.17393742C=	GRCh38
NC_000011.9:g.17415289C= , CM000673.1:g.17415289C=	GRCh37
NC_000011.8:g.17371865C=	NCBI36
NG_008867.1:g.88161G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524561.2:n.4164G=
ENST00000526037.6:n.498G=
ENST00000528374.2:c.1154G=
ENST00000529967.6:n.2902G=
ENST00000532220.2:n.3796G=
ENST00000642611.2:n.5896G=
ENST00000644057.2:n.1139G=
ENST00000645004.2:n.2062G=
ENST00000682051.1:n.4725G=
ENST00000682110.1:n.4778G=
ENST00000682140.1:c.*349G=	ENSP00000507829.1:n.*349G=
ENST00000682185.1:n.5868G=
ENST00000682204.1:c.*2701G=	ENSP00000507094.1:n.*2701G=
ENST00000682215.1:n.5145G=
ENST00000682288.1:c.*2994G=	ENSP00000507506.1:n.*2994G=
ENST00000682442.1:n.4998G=
ENST00000682528.1:n.4855G=
ENST00000682673.1:n.4722G=
ENST00000682805.1:n.5183G=
ENST00000682965.1:c.*985G=	ENSP00000508229.1:n.*985G=
ENST00000683093.1:n.5758G=
ENST00000683136.1:c.4446G=	ENSP00000507768.1:p.Lys1482=
ENST00000683153.1:n.4820G=
ENST00000683365.1:n.4880G=
ENST00000683377.1:n.4674G=
ENST00000683456.1:c.*1700G=	ENSP00000508318.1:n.*1700G=
ENST00000683522.1:n.4860G=
ENST00000683562.1:c.*2628G=	ENSP00000508265.1:n.*2628G=
ENST00000683693.1:n.6239G=
ENST00000683725.1:c.*28G=	ENSP00000507496.1:n.*28G=
ENST00000684010.1:n.4773G=
ENST00000684014.1:n.750G=
ENST00000684157.1:n.5763G=
ENST00000684253.1:n.4681G=
ENST00000684288.1:c.*2735G=	ENSP00000507143.1:n.*2735G=
ENST00000684313.1:n.4210G=
ENST00000684332.1:n.4851G=
ENST00000684371.1:n.4884G=
ENST00000684404.1:n.5806G=
ENST00000684442.1:n.5002G=
ENST00000684555.1:c.*2775G=	ENSP00000507705.1:n.*2775G=
ENST00000684571.1:c.4404G=	ENSP00000506935.1:p.Lys1468=
ENST00000684593.1:c.*4268G=	ENSP00000507005.1:n.*4268G=
ENST00000684711.1:c.*2959G=	ENSP00000506841.1:n.*2959G=
ENST00000302539.9:c.4566G=	ENSP00000303960.4:p.Lys1522=
ENST00000389817.8:c.4563G= MANE Select	ENSP00000374467.4:p.Lys1521=
ENST00000642271.1:c.4560G=	ENSP00000493749.1:p.Lys1520=
ENST00000642579.1:c.2617G=
ENST00000642611.1:n.5781G=
ENST00000642902.1:c.4345G=
ENST00000643260.1:c.4563G=	ENSP00000494450.1:p.Lys1521=
ENST00000643562.1:c.*2685G=	ENSP00000496124.1:n.*2685G=
ENST00000643925.1:c.3185+524G=
ENST00000644057.1:n.722G=
ENST00000644484.1:c.*3949G=	ENSP00000493558.1:n.*3949G=
ENST00000644675.1:c.*2735G=	ENSP00000494567.1:n.*2735G=
ENST00000644757.1:c.*3203-762G=	ENSP00000495085.1:n.*3203-762G=
ENST00000644772.1:c.4629G=	ENSP00000494321.1:p.Lys1543=
ENST00000645004.1:n.2256G=
ENST00000645076.1:c.3658G=
ENST00000645417.1:c.1751G=
ENST00000645744.1:c.*4248G=	ENSP00000494564.1:n.*4248G=
ENST00000645760.1:c.4984G=
ENST00000645884.1:c.*1846G=	ENSP00000495516.1:n.*1846G=
ENST00000646003.1:c.*2585G=	ENSP00000495259.1:n.*2585G=
ENST00000646207.1:c.*3400G=	ENSP00000495025.1:n.*3400G=
ENST00000646276.1:c.*3967G=	ENSP00000496070.1:n.*3967G=
ENST00000646592.1:c.3869G=
ENST00000646902.1:c.4530G=	ENSP00000494101.1:p.Lys1510=
ENST00000646993.1:c.*3001G=	ENSP00000493720.1:n.*3001G=
ENST00000647015.1:c.4314G=	ENSP00000495389.1:p.Lys1438=
ENST00000647086.1:c.*4149G=	ENSP00000493677.1:n.*4149G=
ENST00000647158.1:c.*2850G=	ENSP00000495744.1:n.*2850G=
ENST00000302539.8:c.4566G=	ENSP00000303960.4:p.Lys1522=
ENST00000389817.7:c.4563G=	ENSP00000374467.3:p.Lys1521=
ENST00000525022.1:n.458G=
ENST00000526037.5:n.323G=
ENST00000526168.5:c.351G=
ENST00000531642.5:c.594G=
NM_000352.4:c.4563G=	NP_000343.2:p.Lys1521=
NM_001287174.1:c.4566G=	NP_001274103.1:p.Lys1522=
XM_011520331.1:c.4563G=	XP_011518633.1:p.Lys1521=
XM_011520333.1:c.3063G=	XP_011518635.1:p.Lys1021=
XR_930890.1:n.4525G=
NM_001351295.1:c.4629G=	NP_001338224.1:p.Lys1543=
NM_001351296.1:c.4563G=	NP_001338225.1:p.Lys1521=
NM_001351297.1:c.4560G=	NP_001338226.1:p.Lys1520=
NR_147094.1:n.4858G=
XM_017018197.2:c.4632G=	XP_016873686.1:p.Lys1544=
XM_017018199.1:c.4629G=	XP_016873688.1:p.Lys1543=
XM_017018202.1:c.3129G=	XP_016873691.1:p.Lys1043=
XM_017018204.1:c.2520G=	XP_016873693.1:p.Lys840=
XM_024448668.1:c.2931G=	XP_024304436.1:p.Lys977=
XR_001747945.2:n.4600G=
XR_001747946.2:n.4531G=
XR_002957189.1:n.6314G=
NM_000352.6:c.4563G= MANE Select	NP_000343.2:p.Lys1521=
NM_001287174.2:c.4566G=	NP_001274103.1:p.Lys1522=
NM_001351295.2:c.4629G=	NP_001338224.1:p.Lys1543=
NM_001351296.2:c.4563G=	NP_001338225.1:p.Lys1521=
NM_001351297.2:c.4560G=	NP_001338226.1:p.Lys1520=
NR_147094.2:n.4858G=
NM_001287174.3:c.4566G=	NP_001274103.1:p.Lys1522=