Canonical Allele Identifier: CA1955121974

Gene: ABCC8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17393057A= , CM000673.2:g.17393057A=	GRCh38
NC_000011.9:g.17414604A= , CM000673.1:g.17414604A=	GRCh37
NC_000011.8:g.17371180A=	NCBI36
NG_008867.1:g.88846T=
NG_012446.1:g.603T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524561.2:n.4281T=
ENST00000526037.6:n.615T=
ENST00000528374.2:c.1271T=
ENST00000529967.6:n.3019T=
ENST00000532220.2:n.3913T=
ENST00000642611.2:n.6013T=
ENST00000644057.2:n.1256T=
ENST00000645004.2:n.2179T=
ENST00000682051.1:n.4842T=
ENST00000682110.1:n.4895T=
ENST00000682140.1:c.*466T=	ENSP00000507829.1:n.*466T=
ENST00000682185.1:n.5985T=
ENST00000682204.1:c.*2818T=	ENSP00000507094.1:n.*2818T=
ENST00000682215.1:n.5262T=
ENST00000682288.1:c.*3111T=	ENSP00000507506.1:n.*3111T=
ENST00000682442.1:n.5115T=
ENST00000682528.1:n.4972T=
ENST00000682673.1:n.4839T=
ENST00000682805.1:n.5300T=
ENST00000682965.1:c.*1102T=	ENSP00000508229.1:n.*1102T=
ENST00000683093.1:n.5875T=
ENST00000683136.1:c.4563T=	ENSP00000507768.1:p.Asp1521=
ENST00000683153.1:n.4937T=
ENST00000683365.1:n.4997T=
ENST00000683377.1:n.4791T=
ENST00000683456.1:c.*1817T=	ENSP00000508318.1:n.*1817T=
ENST00000683522.1:n.4977T=
ENST00000683562.1:c.*2745T=	ENSP00000508265.1:n.*2745T=
ENST00000683693.1:n.6356T=
ENST00000683725.1:c.*145T=	ENSP00000507496.1:n.*145T=
ENST00000684010.1:n.4890T=
ENST00000684014.1:n.867T=
ENST00000684157.1:n.5880T=
ENST00000684253.1:n.4798T=
ENST00000684288.1:c.*2852T=	ENSP00000507143.1:n.*2852T=
ENST00000684313.1:n.4327T=
ENST00000684332.1:n.4968T=
ENST00000684371.1:n.5001T=
ENST00000684404.1:n.5923T=
ENST00000684442.1:n.5119T=
ENST00000684555.1:c.*2892T=	ENSP00000507705.1:n.*2892T=
ENST00000684571.1:c.4521T=	ENSP00000506935.1:p.Asp1507=
ENST00000684593.1:c.*4385T=	ENSP00000507005.1:n.*4385T=
ENST00000684711.1:c.*3076T=	ENSP00000506841.1:n.*3076T=
ENST00000302539.9:c.4683T=	ENSP00000303960.4:p.Asp1561=
ENST00000389817.8:c.4680T= MANE Select	ENSP00000374467.4:p.Asp1560=
ENST00000642271.1:c.4677T=	ENSP00000493749.1:p.Asp1559=
ENST00000642579.1:c.2734T=
ENST00000642611.1:n.5898T=
ENST00000642902.1:c.4462T=
ENST00000643260.1:c.4680T=	ENSP00000494450.1:p.Asp1560=
ENST00000643562.1:c.*2802T=	ENSP00000496124.1:n.*2802T=
ENST00000643925.1:c.3257T=
ENST00000644057.1:n.839T=
ENST00000644484.1:c.*4066T=	ENSP00000493558.1:n.*4066T=
ENST00000644675.1:c.*2852T=	ENSP00000494567.1:n.*2852T=
ENST00000644757.1:c.*3203-77T=	ENSP00000495085.1:n.*3203-77T=
ENST00000644772.1:c.4746T=	ENSP00000494321.1:p.Asp1582=
ENST00000645004.1:n.2373T=
ENST00000645076.1:c.3775T=
ENST00000645760.1:c.5101T=
ENST00000645884.1:c.*1963T=	ENSP00000495516.1:n.*1963T=
ENST00000646003.1:c.*2702T=	ENSP00000495259.1:n.*2702T=
ENST00000646207.1:c.*3517T=	ENSP00000495025.1:n.*3517T=
ENST00000646592.1:c.3986T=
ENST00000646902.1:c.4647T=	ENSP00000494101.1:p.Asp1549=
ENST00000646993.1:c.*3118T=	ENSP00000493720.1:n.*3118T=
ENST00000647015.1:c.4431T=	ENSP00000495389.1:p.Asp1477=
ENST00000647086.1:c.*4266T=	ENSP00000493677.1:n.*4266T=
ENST00000302539.8:c.4683T=	ENSP00000303960.4:p.Asp1561=
ENST00000389817.7:c.4680T=	ENSP00000374467.3:p.Asp1560=
ENST00000525022.1:n.659T=
ENST00000526037.5:n.440T=
ENST00000526168.5:c.468T=
ENST00000531642.5:c.711T=
NM_000352.4:c.4680T=	NP_000343.2:p.Asp1560=
NM_001287174.1:c.4683T=	NP_001274103.1:p.Asp1561=
XM_011520331.1:c.4680T=	XP_011518633.1:p.Asp1560=
XM_011520333.1:c.3180T=	XP_011518635.1:p.Asp1060=
XR_930890.1:n.4642T=
NM_001351295.1:c.4746T=	NP_001338224.1:p.Asp1582=
NM_001351296.1:c.4680T=	NP_001338225.1:p.Asp1560=
NM_001351297.1:c.4677T=	NP_001338226.1:p.Asp1559=
NR_147094.1:n.4975T=
XM_017018197.2:c.4749T=	XP_016873686.1:p.Asp1583=
XM_017018199.1:c.4746T=	XP_016873688.1:p.Asp1582=
XM_017018202.1:c.3246T=	XP_016873691.1:p.Asp1082=
XM_017018204.1:c.2637T=	XP_016873693.1:p.Asp879=
XM_024448668.1:c.3048T=	XP_024304436.1:p.Asp1016=
XR_001747945.2:n.4717T=
XR_001747946.2:n.4648T=
XR_002957189.1:n.6431T=
NM_000352.6:c.4680T= MANE Select	NP_000343.2:p.Asp1560=
NM_001287174.2:c.4683T=	NP_001274103.1:p.Asp1561=
NM_001351295.2:c.4746T=	NP_001338224.1:p.Asp1582=
NM_001351296.2:c.4680T=	NP_001338225.1:p.Asp1560=
NM_001351297.2:c.4677T=	NP_001338226.1:p.Asp1559=
NR_147094.2:n.4975T=
NM_001287174.3:c.4683T=	NP_001274103.1:p.Asp1561=