Canonical Allele Identifier: CA1955122293

Gene: ABCC8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17393702T= , CM000673.2:g.17393702T=	GRCh38
NC_000011.9:g.17415249T= , CM000673.1:g.17415249T=	GRCh37
NC_000011.8:g.17371825T=	NCBI36
NG_008867.1:g.88201A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524561.2:n.4204A=
ENST00000526037.6:n.538A=
ENST00000528374.2:c.1194A=
ENST00000529967.6:n.2942A=
ENST00000532220.2:n.3836A=
ENST00000642611.2:n.5936A=
ENST00000644057.2:n.1179A=
ENST00000645004.2:n.2102A=
ENST00000682051.1:n.4765A=
ENST00000682110.1:n.4818A=
ENST00000682140.1:c.*389A=	ENSP00000507829.1:n.*389A=
ENST00000682185.1:n.5908A=
ENST00000682204.1:c.*2741A=	ENSP00000507094.1:n.*2741A=
ENST00000682215.1:n.5185A=
ENST00000682288.1:c.*3034A=	ENSP00000507506.1:n.*3034A=
ENST00000682442.1:n.5038A=
ENST00000682528.1:n.4895A=
ENST00000682673.1:n.4762A=
ENST00000682805.1:n.5223A=
ENST00000682965.1:c.*1025A=	ENSP00000508229.1:n.*1025A=
ENST00000683093.1:n.5798A=
ENST00000683136.1:c.4486A=	ENSP00000507768.1:p.Ile1496=
ENST00000683153.1:n.4860A=
ENST00000683365.1:n.4920A=
ENST00000683377.1:n.4714A=
ENST00000683456.1:c.*1740A=	ENSP00000508318.1:n.*1740A=
ENST00000683522.1:n.4900A=
ENST00000683562.1:c.*2668A=	ENSP00000508265.1:n.*2668A=
ENST00000683693.1:n.6279A=
ENST00000683725.1:c.*68A=	ENSP00000507496.1:n.*68A=
ENST00000684010.1:n.4813A=
ENST00000684014.1:n.790A=
ENST00000684157.1:n.5803A=
ENST00000684253.1:n.4721A=
ENST00000684288.1:c.*2775A=	ENSP00000507143.1:n.*2775A=
ENST00000684313.1:n.4250A=
ENST00000684332.1:n.4891A=
ENST00000684371.1:n.4924A=
ENST00000684404.1:n.5846A=
ENST00000684442.1:n.5042A=
ENST00000684555.1:c.*2815A=	ENSP00000507705.1:n.*2815A=
ENST00000684571.1:c.4444A=	ENSP00000506935.1:p.Ile1482=
ENST00000684593.1:c.*4308A=	ENSP00000507005.1:n.*4308A=
ENST00000684711.1:c.*2999A=	ENSP00000506841.1:n.*2999A=
ENST00000302539.9:c.4606A=	ENSP00000303960.4:p.Ile1536=
ENST00000389817.8:c.4603A= MANE Select	ENSP00000374467.4:p.Ile1535=
ENST00000642271.1:c.4600A=	ENSP00000493749.1:p.Ile1534=
ENST00000642579.1:c.2657A=
ENST00000642611.1:n.5821A=
ENST00000642902.1:c.4385A=
ENST00000643260.1:c.4603A=	ENSP00000494450.1:p.Ile1535=
ENST00000643562.1:c.*2725A=	ENSP00000496124.1:n.*2725A=
ENST00000643925.1:c.3185+564A=
ENST00000644057.1:n.762A=
ENST00000644484.1:c.*3989A=	ENSP00000493558.1:n.*3989A=
ENST00000644675.1:c.*2775A=	ENSP00000494567.1:n.*2775A=
ENST00000644757.1:c.*3203-722A=	ENSP00000495085.1:n.*3203-722A=
ENST00000644772.1:c.4669A=	ENSP00000494321.1:p.Ile1557=
ENST00000645004.1:n.2296A=
ENST00000645076.1:c.3698A=
ENST00000645417.1:c.1791A=
ENST00000645744.1:c.*4288A=	ENSP00000494564.1:n.*4288A=
ENST00000645760.1:c.5024A=
ENST00000645884.1:c.*1886A=	ENSP00000495516.1:n.*1886A=
ENST00000646003.1:c.*2625A=	ENSP00000495259.1:n.*2625A=
ENST00000646207.1:c.*3440A=	ENSP00000495025.1:n.*3440A=
ENST00000646276.1:c.*4007A=	ENSP00000496070.1:n.*4007A=
ENST00000646592.1:c.3909A=
ENST00000646902.1:c.4570A=	ENSP00000494101.1:p.Ile1524=
ENST00000646993.1:c.*3041A=	ENSP00000493720.1:n.*3041A=
ENST00000647015.1:c.4354A=	ENSP00000495389.1:p.Ile1452=
ENST00000647086.1:c.*4189A=	ENSP00000493677.1:n.*4189A=
ENST00000647158.1:c.*2890A=	ENSP00000495744.1:n.*2890A=
ENST00000302539.8:c.4606A=	ENSP00000303960.4:p.Ile1536=
ENST00000389817.7:c.4603A=	ENSP00000374467.3:p.Ile1535=
ENST00000525022.1:n.498A=
ENST00000526037.5:n.363A=
ENST00000526168.5:c.391A=
ENST00000531642.5:c.634A=
NM_000352.4:c.4603A=	NP_000343.2:p.Ile1535=
NM_001287174.1:c.4606A=	NP_001274103.1:p.Ile1536=
XM_011520331.1:c.4603A=	XP_011518633.1:p.Ile1535=
XM_011520333.1:c.3103A=	XP_011518635.1:p.Ile1035=
XR_930890.1:n.4565A=
NM_001351295.1:c.4669A=	NP_001338224.1:p.Ile1557=
NM_001351296.1:c.4603A=	NP_001338225.1:p.Ile1535=
NM_001351297.1:c.4600A=	NP_001338226.1:p.Ile1534=
NR_147094.1:n.4898A=
XM_017018197.2:c.4672A=	XP_016873686.1:p.Ile1558=
XM_017018199.1:c.4669A=	XP_016873688.1:p.Ile1557=
XM_017018202.1:c.3169A=	XP_016873691.1:p.Ile1057=
XM_017018204.1:c.2560A=	XP_016873693.1:p.Ile854=
XM_024448668.1:c.2971A=	XP_024304436.1:p.Ile991=
XR_001747945.2:n.4640A=
XR_001747946.2:n.4571A=
XR_002957189.1:n.6354A=
NM_000352.6:c.4603A= MANE Select	NP_000343.2:p.Ile1535=
NM_001287174.2:c.4606A=	NP_001274103.1:p.Ile1536=
NM_001351295.2:c.4669A=	NP_001338224.1:p.Ile1557=
NM_001351296.2:c.4603A=	NP_001338225.1:p.Ile1535=
NM_001351297.2:c.4600A=	NP_001338226.1:p.Ile1534=
NR_147094.2:n.4898A=
NM_001287174.3:c.4606A=	NP_001274103.1:p.Ile1536=