Canonical Allele Identifier: CA1955154571

Gene: ABCC8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17461811G= , CM000673.2:g.17461811G=	GRCh38
NC_000011.9:g.17483358G= , CM000673.1:g.17483358G=	GRCh37
NC_000011.8:g.17439934G=	NCBI36
NG_008867.1:g.20092C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524561.2:n.648+1627C=
ENST00000526002.2:n.607C=
ENST00000528202.6:n.663C=
ENST00000642611.2:n.663C=
ENST00000682051.1:n.607C=
ENST00000682091.1:n.663C=
ENST00000682110.1:n.663C=
ENST00000682140.1:c.594C=	ENSP00000507829.1:p.Phe198=
ENST00000682199.1:n.663C=
ENST00000682204.1:c.594C=	ENSP00000507094.1:p.Phe198=
ENST00000682215.1:n.663C=
ENST00000682288.1:c.594C=	ENSP00000507506.1:p.Phe198=
ENST00000682442.1:n.694C=
ENST00000682528.1:n.663C=
ENST00000682673.1:n.607C=
ENST00000682805.1:n.663C=
ENST00000682863.1:n.663C=
ENST00000682965.1:c.594C=	ENSP00000508229.1:p.Phe198=
ENST00000683093.1:n.663C=
ENST00000683136.1:c.594C=	ENSP00000507768.1:p.Phe198=
ENST00000683153.1:n.663C=
ENST00000683253.1:n.668C=
ENST00000683365.1:n.663C=
ENST00000683377.1:n.663C=
ENST00000683456.1:c.594C=	ENSP00000508318.1:p.Phe198=
ENST00000683522.1:n.663C=
ENST00000683531.1:n.663C=
ENST00000683562.1:c.594C=	ENSP00000508265.1:p.Phe198=
ENST00000683693.1:n.663C=
ENST00000683725.1:c.594C=	ENSP00000507496.1:p.Phe198=
ENST00000684010.1:n.663C=
ENST00000684157.1:n.663C=
ENST00000684221.1:n.524C=
ENST00000684253.1:n.712C=
ENST00000684288.1:c.594C=	ENSP00000507143.1:p.Phe198=
ENST00000684313.1:n.690C=
ENST00000684332.1:n.663C=
ENST00000684371.1:n.607C=
ENST00000684404.1:n.663C=
ENST00000684442.1:n.663C=
ENST00000684555.1:c.594C=	ENSP00000507705.1:p.Phe198=
ENST00000684571.1:c.594C=	ENSP00000506935.1:p.Phe198=
ENST00000684593.1:c.*299C=	ENSP00000507005.1:n.*299C=
ENST00000684711.1:c.594C=	ENSP00000506841.1:p.Phe198=
ENST00000302539.9:c.594C=	ENSP00000303960.4:p.Phe198=
ENST00000389817.8:c.594C= MANE Select	ENSP00000374467.4:p.Phe198=
ENST00000532728.6:c.473C=
ENST00000635881.1:n.625C=
ENST00000642271.1:c.594C=	ENSP00000493749.1:p.Phe198=
ENST00000642611.1:n.548C=
ENST00000642902.1:c.578C=
ENST00000643260.1:c.594C=	ENSP00000494450.1:p.Phe198=
ENST00000643562.1:c.594C=	ENSP00000496124.1:p.Phe198=
ENST00000644472.1:c.594C=	ENSP00000495378.1:p.Phe198=
ENST00000644484.1:c.594C=	ENSP00000493558.1:p.Phe198=
ENST00000644542.1:c.*299C=	ENSP00000495532.1:n.*299C=
ENST00000644675.1:c.594C=	ENSP00000494567.1:p.Phe198=
ENST00000644757.1:c.594C=	ENSP00000495085.1:p.Phe198=
ENST00000644772.1:c.594C=	ENSP00000494321.1:p.Phe198=
ENST00000645744.1:c.594C=	ENSP00000494564.1:p.Phe198=
ENST00000645760.1:c.767C=
ENST00000645884.1:c.594C=	ENSP00000495516.1:p.Phe198=
ENST00000646003.1:c.594C=	ENSP00000495259.1:p.Phe198=
ENST00000646207.1:c.594C=	ENSP00000495025.1:p.Phe198=
ENST00000646276.1:c.573C=	ENSP00000496070.1:p.Phe191=
ENST00000646737.1:c.472C=	ENSP00000494874.1:p.Gln158=
ENST00000646902.1:c.594C=	ENSP00000494101.1:p.Phe198=
ENST00000646993.1:c.594C=	ENSP00000493720.1:p.Phe198=
ENST00000647013.1:c.492C=	ENSP00000496741.1:p.Phe164=
ENST00000647015.1:c.594C=	ENSP00000495389.1:p.Phe198=
ENST00000647086.1:c.594C=	ENSP00000493677.1:p.Phe198=
ENST00000647158.1:c.594C=	ENSP00000495744.1:p.Phe198=
ENST00000302539.8:c.594C=	ENSP00000303960.4:p.Phe198=
ENST00000389817.7:c.594C=	ENSP00000374467.3:p.Phe198=
ENST00000527905.5:c.594C=	ENSP00000431653.1:p.Phe198=
ENST00000532728.5:n.625C=
NM_000352.4:c.594C=	NP_000343.2:p.Phe198=
NM_001287174.1:c.594C=	NP_001274103.1:p.Phe198=
XM_011520331.1:c.594C=	XP_011518633.1:p.Phe198=
XM_011520332.1:c.594C=	XP_011518634.1:p.Phe198=
XM_011520334.1:c.594C=	XP_011518636.1:p.Phe198=
XR_930890.1:n.657C=
XR_930891.1:n.657C=
XR_930892.1:n.657C=
XR_930893.1:n.657C=
NM_001351295.1:c.594C=	NP_001338224.1:p.Phe198=
NM_001351296.1:c.594C=	NP_001338225.1:p.Phe198=
NM_001351297.1:c.594C=	NP_001338226.1:p.Phe198=
NR_147094.1:n.663C=
XM_017018197.2:c.594C=	XP_016873686.1:p.Phe198=
XM_017018199.1:c.594C=	XP_016873688.1:p.Phe198=
XM_017018201.2:c.594C=	XP_016873690.1:p.Phe198=
XM_017018202.1:c.-924C=	XP_016873691.1:n.-924C=
XM_024448668.1:c.-2050C=	XP_024304436.1:n.-2050C=
XR_001747945.2:n.666C=
XR_001747946.2:n.666C=
XR_002957189.1:n.666C=
NM_000352.6:c.594C= MANE Select	NP_000343.2:p.Phe198=
NM_001287174.2:c.594C=	NP_001274103.1:p.Phe198=
NM_001351295.2:c.594C=	NP_001338224.1:p.Phe198=
NM_001351296.2:c.594C=	NP_001338225.1:p.Phe198=
NM_001351297.2:c.594C=	NP_001338226.1:p.Phe198=
NR_147094.2:n.663C=
NM_001287174.3:c.594C=	NP_001274103.1:p.Phe198=