Canonical Allele Identifier: CA1955122305

Gene: ABCC8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17393735T= , CM000673.2:g.17393735T=	GRCh38
NC_000011.9:g.17415282T= , CM000673.1:g.17415282T=	GRCh37
NC_000011.8:g.17371858T=	NCBI36
NG_008867.1:g.88168A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524561.2:n.4171A=
ENST00000526037.6:n.505A=
ENST00000528374.2:c.1161A=
ENST00000529967.6:n.2909A=
ENST00000532220.2:n.3803A=
ENST00000642611.2:n.5903A=
ENST00000644057.2:n.1146A=
ENST00000645004.2:n.2069A=
ENST00000682051.1:n.4732A=
ENST00000682110.1:n.4785A=
ENST00000682140.1:c.*356A=	ENSP00000507829.1:n.*356A=
ENST00000682185.1:n.5875A=
ENST00000682204.1:c.*2708A=	ENSP00000507094.1:n.*2708A=
ENST00000682215.1:n.5152A=
ENST00000682288.1:c.*3001A=	ENSP00000507506.1:n.*3001A=
ENST00000682442.1:n.5005A=
ENST00000682528.1:n.4862A=
ENST00000682673.1:n.4729A=
ENST00000682805.1:n.5190A=
ENST00000682965.1:c.*992A=	ENSP00000508229.1:n.*992A=
ENST00000683093.1:n.5765A=
ENST00000683136.1:c.4453A=	ENSP00000507768.1:p.Met1485=
ENST00000683153.1:n.4827A=
ENST00000683365.1:n.4887A=
ENST00000683377.1:n.4681A=
ENST00000683456.1:c.*1707A=	ENSP00000508318.1:n.*1707A=
ENST00000683522.1:n.4867A=
ENST00000683562.1:c.*2635A=	ENSP00000508265.1:n.*2635A=
ENST00000683693.1:n.6246A=
ENST00000683725.1:c.*35A=	ENSP00000507496.1:n.*35A=
ENST00000684010.1:n.4780A=
ENST00000684014.1:n.757A=
ENST00000684157.1:n.5770A=
ENST00000684253.1:n.4688A=
ENST00000684288.1:c.*2742A=	ENSP00000507143.1:n.*2742A=
ENST00000684313.1:n.4217A=
ENST00000684332.1:n.4858A=
ENST00000684371.1:n.4891A=
ENST00000684404.1:n.5813A=
ENST00000684442.1:n.5009A=
ENST00000684555.1:c.*2782A=	ENSP00000507705.1:n.*2782A=
ENST00000684571.1:c.4411A=	ENSP00000506935.1:p.Met1471=
ENST00000684593.1:c.*4275A=	ENSP00000507005.1:n.*4275A=
ENST00000684711.1:c.*2966A=	ENSP00000506841.1:n.*2966A=
ENST00000302539.9:c.4573A=	ENSP00000303960.4:p.Met1525=
ENST00000389817.8:c.4570A= MANE Select	ENSP00000374467.4:p.Met1524=
ENST00000642271.1:c.4567A=	ENSP00000493749.1:p.Met1523=
ENST00000642579.1:c.2624A=
ENST00000642611.1:n.5788A=
ENST00000642902.1:c.4352A=
ENST00000643260.1:c.4570A=	ENSP00000494450.1:p.Met1524=
ENST00000643562.1:c.*2692A=	ENSP00000496124.1:n.*2692A=
ENST00000643925.1:c.3185+531A=
ENST00000644057.1:n.729A=
ENST00000644484.1:c.*3956A=	ENSP00000493558.1:n.*3956A=
ENST00000644675.1:c.*2742A=	ENSP00000494567.1:n.*2742A=
ENST00000644757.1:c.*3203-755A=	ENSP00000495085.1:n.*3203-755A=
ENST00000644772.1:c.4636A=	ENSP00000494321.1:p.Met1546=
ENST00000645004.1:n.2263A=
ENST00000645076.1:c.3665A=
ENST00000645417.1:c.1758A=
ENST00000645744.1:c.*4255A=	ENSP00000494564.1:n.*4255A=
ENST00000645760.1:c.4991A=
ENST00000645884.1:c.*1853A=	ENSP00000495516.1:n.*1853A=
ENST00000646003.1:c.*2592A=	ENSP00000495259.1:n.*2592A=
ENST00000646207.1:c.*3407A=	ENSP00000495025.1:n.*3407A=
ENST00000646276.1:c.*3974A=	ENSP00000496070.1:n.*3974A=
ENST00000646592.1:c.3876A=
ENST00000646902.1:c.4537A=	ENSP00000494101.1:p.Met1513=
ENST00000646993.1:c.*3008A=	ENSP00000493720.1:n.*3008A=
ENST00000647015.1:c.4321A=	ENSP00000495389.1:p.Met1441=
ENST00000647086.1:c.*4156A=	ENSP00000493677.1:n.*4156A=
ENST00000647158.1:c.*2857A=	ENSP00000495744.1:n.*2857A=
ENST00000302539.8:c.4573A=	ENSP00000303960.4:p.Met1525=
ENST00000389817.7:c.4570A=	ENSP00000374467.3:p.Met1524=
ENST00000525022.1:n.465A=
ENST00000526037.5:n.330A=
ENST00000526168.5:c.358A=
ENST00000531642.5:c.601A=
NM_000352.4:c.4570A=	NP_000343.2:p.Met1524=
NM_001287174.1:c.4573A=	NP_001274103.1:p.Met1525=
XM_011520331.1:c.4570A=	XP_011518633.1:p.Met1524=
XM_011520333.1:c.3070A=	XP_011518635.1:p.Met1024=
XR_930890.1:n.4532A=
NM_001351295.1:c.4636A=	NP_001338224.1:p.Met1546=
NM_001351296.1:c.4570A=	NP_001338225.1:p.Met1524=
NM_001351297.1:c.4567A=	NP_001338226.1:p.Met1523=
NR_147094.1:n.4865A=
XM_017018197.2:c.4639A=	XP_016873686.1:p.Met1547=
XM_017018199.1:c.4636A=	XP_016873688.1:p.Met1546=
XM_017018202.1:c.3136A=	XP_016873691.1:p.Met1046=
XM_017018204.1:c.2527A=	XP_016873693.1:p.Met843=
XM_024448668.1:c.2938A=	XP_024304436.1:p.Met980=
XR_001747945.2:n.4607A=
XR_001747946.2:n.4538A=
XR_002957189.1:n.6321A=
NM_000352.6:c.4570A= MANE Select	NP_000343.2:p.Met1524=
NM_001287174.2:c.4573A=	NP_001274103.1:p.Met1525=
NM_001351295.2:c.4636A=	NP_001338224.1:p.Met1546=
NM_001351296.2:c.4570A=	NP_001338225.1:p.Met1524=
NM_001351297.2:c.4567A=	NP_001338226.1:p.Met1523=
NR_147094.2:n.4865A=
NM_001287174.3:c.4573A=	NP_001274103.1:p.Met1525=