Canonical Allele Identifier: CA1955123266

Gene: ABCC8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17395717C= , CM000673.2:g.17395717C=	GRCh38
NC_000011.9:g.17417264C= , CM000673.1:g.17417264C=	GRCh37
NC_000011.8:g.17373840C=	NCBI36
NG_008867.1:g.86186G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524561.2:n.3801G=
ENST00000528374.2:c.791G=
ENST00000529967.6:n.2539G=
ENST00000532220.2:n.3433G=
ENST00000642611.2:n.5533G=
ENST00000644057.2:n.776G=
ENST00000645004.2:n.1699G=
ENST00000682051.1:n.4362G=
ENST00000682110.1:n.4415G=
ENST00000682140.1:c.4066G=	ENSP00000507829.1:p.Ala1356=
ENST00000682185.1:n.5505G=
ENST00000682204.1:c.*2338G=	ENSP00000507094.1:n.*2338G=
ENST00000682215.1:n.4782G=
ENST00000682288.1:c.*2631G=	ENSP00000507506.1:n.*2631G=
ENST00000682442.1:n.4635G=
ENST00000682528.1:n.4492G=
ENST00000682673.1:n.4359G=
ENST00000682805.1:n.4820G=
ENST00000682965.1:c.*622G=	ENSP00000508229.1:n.*622G=
ENST00000683093.1:n.5499G=
ENST00000683136.1:c.4083G=	ENSP00000507768.1:p.Gly1361=
ENST00000683153.1:n.4457G=
ENST00000683365.1:n.4517G=
ENST00000683377.1:n.4415G=
ENST00000683456.1:c.*1337G=	ENSP00000508318.1:n.*1337G=
ENST00000683522.1:n.4415G=
ENST00000683562.1:c.*2369G=	ENSP00000508265.1:n.*2369G=
ENST00000683693.1:n.5980G=
ENST00000683725.1:c.4200G=	ENSP00000507496.1:p.Gly1400=
ENST00000684010.1:n.4410G=
ENST00000684157.1:n.5400G=
ENST00000684253.1:n.4318G=
ENST00000684288.1:c.*2372G=	ENSP00000507143.1:n.*2372G=
ENST00000684313.1:n.3847G=
ENST00000684332.1:n.4488G=
ENST00000684371.1:n.4521G=
ENST00000684404.1:n.5443G=
ENST00000684442.1:n.4639G=
ENST00000684555.1:c.*2412G=	ENSP00000507705.1:n.*2412G=
ENST00000684571.1:c.4041G=	ENSP00000506935.1:p.Gly1347=
ENST00000684593.1:c.*3905G=	ENSP00000507005.1:n.*3905G=
ENST00000684711.1:c.*2596G=	ENSP00000506841.1:n.*2596G=
ENST00000302539.9:c.4203G=	ENSP00000303960.4:p.Gly1401=
ENST00000389817.8:c.4200G= MANE Select	ENSP00000374467.4:p.Gly1400=
ENST00000642271.1:c.4197G=	ENSP00000493749.1:p.Gly1399=
ENST00000642579.1:c.2254G=
ENST00000642611.1:n.5418G=
ENST00000642902.1:c.3982G=
ENST00000643260.1:c.4200G=	ENSP00000494450.1:p.Gly1400=
ENST00000643562.1:c.*2322G=	ENSP00000496124.1:n.*2322G=
ENST00000643925.1:c.2840G=
ENST00000644057.1:n.277G=
ENST00000644484.1:c.*3586G=	ENSP00000493558.1:n.*3586G=
ENST00000644675.1:c.*2372G=	ENSP00000494567.1:n.*2372G=
ENST00000644757.1:c.*3202+547G=	ENSP00000495085.1:n.*3202+547G=
ENST00000644772.1:c.4266G=	ENSP00000494321.1:p.Gly1422=
ENST00000645004.1:n.1893G=
ENST00000645076.1:c.3399G=
ENST00000645417.1:c.1388G=
ENST00000645744.1:c.*3964-79G=	ENSP00000494564.1:n.*3964-79G=
ENST00000645760.1:c.4621G=
ENST00000645884.1:c.*1483G=	ENSP00000495516.1:n.*1483G=
ENST00000646003.1:c.*2301-79G=	ENSP00000495259.1:n.*2301-79G=
ENST00000646207.1:c.*3037G=	ENSP00000495025.1:n.*3037G=
ENST00000646276.1:c.*3604G=	ENSP00000496070.1:n.*3604G=
ENST00000646592.1:c.3506G=
ENST00000646902.1:c.4167G=	ENSP00000494101.1:p.Gly1389=
ENST00000646993.1:c.*2742G=	ENSP00000493720.1:n.*2742G=
ENST00000647013.1:c.4206G=	ENSP00000496741.1:n.4206G=
ENST00000647015.1:c.3951G=	ENSP00000495389.1:p.Gly1317=
ENST00000647086.1:c.*3786G=	ENSP00000493677.1:n.*3786G=
ENST00000647158.1:c.*2487G=	ENSP00000495744.1:n.*2487G=
ENST00000302539.8:c.4203G=	ENSP00000303960.4:p.Gly1401=
ENST00000389817.7:c.4200G=	ENSP00000374467.3:p.Gly1400=
ENST00000525022.1:n.199G=
ENST00000526037.5:n.64G=
ENST00000526168.5:c.67-79G=
ENST00000531642.5:c.36G=
NM_000352.4:c.4200G=	NP_000343.2:p.Gly1400=
NM_001287174.1:c.4203G=	NP_001274103.1:p.Gly1401=
XM_011520331.1:c.4200G=	XP_011518633.1:p.Gly1400=
XM_011520332.1:c.4203G=	XP_011518634.1:p.Gly1401=
XM_011520333.1:c.2700G=	XP_011518635.1:p.Gly900=
XR_930890.1:n.4266G=
NM_001351295.1:c.4266G=	NP_001338224.1:p.Gly1422=
NM_001351296.1:c.4200G=	NP_001338225.1:p.Gly1400=
NM_001351297.1:c.4197G=	NP_001338226.1:p.Gly1399=
NR_147094.1:n.4495G=
XM_017018197.2:c.4269G=	XP_016873686.1:p.Gly1423=
XM_017018199.1:c.4266G=	XP_016873688.1:p.Gly1422=
XM_017018201.2:c.4269G=	XP_016873690.1:p.Gly1423=
XM_017018202.1:c.2766G=	XP_016873691.1:p.Gly922=
XM_017018204.1:c.2157G=	XP_016873693.1:p.Gly719=
XM_024448668.1:c.2568G=	XP_024304436.1:p.Gly856=
XR_001747945.2:n.4341G=
XR_001747946.2:n.4272G=
XR_002957189.1:n.6055G=
NM_000352.6:c.4200G= MANE Select	NP_000343.2:p.Gly1400=
NM_001287174.2:c.4203G=	NP_001274103.1:p.Gly1401=
NM_001351295.2:c.4266G=	NP_001338224.1:p.Gly1422=
NM_001351296.2:c.4200G=	NP_001338225.1:p.Gly1400=
NM_001351297.2:c.4197G=	NP_001338226.1:p.Gly1399=
NR_147094.2:n.4495G=
NM_001287174.3:c.4203G=	NP_001274103.1:p.Gly1401=