Canonical Allele Identifier: CA2612643176

Gene: ABCC8

Linked Data

• gnomAD v4: 11-17397088-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17397088G>A , CM000673.2:g.17397088G>A	GRCh38
NC_000011.9:g.17418635G>A , CM000673.1:g.17418635G>A	GRCh37
NC_000011.8:g.17375211G>A	NCBI36
NG_008867.1:g.84815C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524561.2:n.3548C>T
ENST00000528374.2:c.568-30C>T
ENST00000529967.6:n.2328-42C>T
ENST00000532220.2:n.2195C>T
ENST00000642611.2:n.4162C>T
ENST00000644057.2:n.432-42C>T
ENST00000645004.2:n.1488-42C>T
ENST00000682051.1:n.4109C>T
ENST00000682110.1:n.4162C>T
ENST00000682140.1:c.3985+105C>T	ENSP00000507829.1:n.3985+105C>T
ENST00000682185.1:n.5294-42C>T
ENST00000682204.1:c.*2127-42C>T	ENSP00000507094.1:n.*2127-42C>T
ENST00000682215.1:n.4529C>T
ENST00000682288.1:c.*2420-42C>T	ENSP00000507506.1:n.*2420-42C>T
ENST00000682442.1:n.4382C>T
ENST00000682528.1:n.4239C>T
ENST00000682673.1:n.4106C>T
ENST00000682805.1:n.4529C>T
ENST00000682965.1:c.*411-42C>T	ENSP00000508229.1:n.*411-42C>T
ENST00000683093.1:n.4261C>T
ENST00000683136.1:c.3872-42C>T	ENSP00000507768.1:n.3872-42C>T
ENST00000683153.1:n.4204C>T
ENST00000683365.1:n.4264C>T
ENST00000683377.1:n.4162C>T
ENST00000683456.1:c.*1126-42C>T	ENSP00000508318.1:n.*1126-42C>T
ENST00000683522.1:n.4162C>T
ENST00000683562.1:c.*2158-42C>T	ENSP00000508265.1:n.*2158-42C>T
ENST00000683693.1:n.4609C>T
ENST00000683725.1:c.3989-42C>T	ENSP00000507496.1:n.3989-42C>T
ENST00000684010.1:n.4157C>T
ENST00000684157.1:n.4162C>T
ENST00000684253.1:n.4065C>T
ENST00000684288.1:c.*2161-42C>T	ENSP00000507143.1:n.*2161-42C>T
ENST00000684313.1:n.3594C>T
ENST00000684332.1:n.4235C>T
ENST00000684371.1:n.4268C>T
ENST00000684404.1:n.4205C>T
ENST00000684442.1:n.4428-42C>T
ENST00000684555.1:c.*2201-42C>T	ENSP00000507705.1:n.*2201-42C>T
ENST00000684571.1:c.3830-42C>T	ENSP00000506935.1:n.3830-42C>T
ENST00000684593.1:c.*3694-42C>T	ENSP00000507005.1:n.*3694-42C>T
ENST00000684711.1:c.*2385-42C>T	ENSP00000506841.1:n.*2385-42C>T
ENST00000302539.9:c.3992-42C>T	ENSP00000303960.4:n.3992-42C>T
ENST00000389817.8:c.3989-42C>T MANE Select	ENSP00000374467.4:n.3989-42C>T
ENST00000642271.1:c.3986-42C>T	ENSP00000493749.1:n.3986-42C>T
ENST00000642579.1:c.2073-72C>T
ENST00000642611.1:n.4047C>T
ENST00000642902.1:c.3771-42C>T
ENST00000643260.1:c.3989-42C>T	ENSP00000494450.1:n.3989-42C>T
ENST00000643562.1:c.*2069C>T	ENSP00000496124.1:n.*2069C>T
ENST00000643925.1:c.2587C>T
ENST00000644057.1:n.24C>T
ENST00000644484.1:c.*2348C>T	ENSP00000493558.1:n.*2348C>T
ENST00000644675.1:c.*2161-42C>T	ENSP00000494567.1:n.*2161-42C>T
ENST00000644757.1:c.*2378C>T	ENSP00000495085.1:n.*2378C>T
ENST00000644772.1:c.4055-42C>T	ENSP00000494321.1:n.4055-42C>T
ENST00000645004.1:n.1602C>T
ENST00000645076.1:c.3188-42C>T
ENST00000645417.1:c.1177-42C>T
ENST00000645744.1:c.*2727C>T	ENSP00000494564.1:n.*2727C>T
ENST00000645760.1:c.4368C>T
ENST00000645884.1:c.*1230C>T	ENSP00000495516.1:n.*1230C>T
ENST00000646003.1:c.*2049C>T	ENSP00000495259.1:n.*2049C>T
ENST00000646207.1:c.*2826-42C>T	ENSP00000495025.1:n.*2826-42C>T
ENST00000646276.1:c.*2366C>T	ENSP00000496070.1:n.*2366C>T
ENST00000646592.1:c.3295-42C>T
ENST00000646902.1:c.3986-72C>T	ENSP00000494101.1:n.3986-72C>T
ENST00000646993.1:c.*2489C>T	ENSP00000493720.1:n.*2489C>T
ENST00000647013.1:c.3995-42C>T	ENSP00000496741.1:n.3995-42C>T
ENST00000647015.1:c.3740-42C>T	ENSP00000495389.1:n.3740-42C>T
ENST00000647086.1:c.*3605-72C>T	ENSP00000493677.1:n.*3605-72C>T
ENST00000647158.1:c.*2234C>T	ENSP00000495744.1:n.*2234C>T
ENST00000302539.8:c.3992-42C>T	ENSP00000303960.4:n.3992-42C>T
ENST00000389817.7:c.3989-42C>T	ENSP00000374467.3:n.3989-42C>T
ENST00000527905.5:c.*969C>T	ENSP00000431653.1:n.*969C>T
ENST00000528374.1:c.459-30C>T
ENST00000531137.1:n.512C>T
ENST00000531891.1:c.357-72C>T
ENST00000532220.1:n.421C>T
NM_000352.4:c.3989-42C>T	NP_000343.2:n.3989-42C>T
NM_001287174.1:c.3992-42C>T	NP_001274103.1:n.3992-42C>T
XM_011520331.1:c.3989-42C>T	XP_011518633.1:n.3989-42C>T
XM_011520332.1:c.3992-42C>T	XP_011518634.1:n.3992-42C>T
XM_011520333.1:c.2489-42C>T	XP_011518635.1:n.2489-42C>T
XR_930890.1:n.4055-42C>T
NM_001351295.1:c.4055-42C>T	NP_001338224.1:n.4055-42C>T
NM_001351296.1:c.3989-42C>T	NP_001338225.1:n.3989-42C>T
NM_001351297.1:c.3986-42C>T	NP_001338226.1:n.3986-42C>T
NR_147094.1:n.4242C>T
XM_017018197.2:c.4058-42C>T	XP_016873686.1:n.4058-42C>T
XM_017018199.1:c.4055-42C>T	XP_016873688.1:n.4055-42C>T
XM_017018201.2:c.4058-42C>T	XP_016873690.1:n.4058-42C>T
XM_017018202.1:c.2555-42C>T	XP_016873691.1:n.2555-42C>T
XM_017018204.1:c.1946-42C>T	XP_016873693.1:n.1946-42C>T
XM_024448668.1:c.2357-42C>T	XP_024304436.1:n.2357-42C>T
XR_001747945.2:n.4130-42C>T
XR_001747946.2:n.4061-42C>T
XR_002957189.1:n.4684C>T
NM_000352.6:c.3989-42C>T MANE Select	NP_000343.2:n.3989-42C>T
NM_001287174.2:c.3992-42C>T	NP_001274103.1:n.3992-42C>T
NM_001351295.2:c.4055-42C>T	NP_001338224.1:n.4055-42C>T
NM_001351296.2:c.3989-42C>T	NP_001338225.1:n.3989-42C>T
NM_001351297.2:c.3986-42C>T	NP_001338226.1:n.3986-42C>T
NR_147094.2:n.4242C>T
NM_001287174.3:c.3992-42C>T	NP_001274103.1:n.3992-42C>T