Canonical Allele Identifier: CA5902802

Gene: ABCC8

Linked Data

• dbSNP Id: rs775827563
• ExAC: 11:17426156 C / T
• gnomAD v2: 11-17426156-C-T
• gnomAD v3: 11-17404609-C-T
• gnomAD v4: 11-17404609-C-T
• MyVariant Identifiers: chr11:g.17426156C>T (hg19) ; chr11:g.17404609C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17404609C>T , CM000673.2:g.17404609C>T	GRCh38
NC_000011.9:g.17426156C>T , CM000673.1:g.17426156C>T	GRCh37
NC_000011.8:g.17382732C>T	NCBI36
NG_008867.1:g.77294G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524561.2:n.3029G>A
ENST00000528374.2:c.39G>A
ENST00000529967.6:n.1799G>A
ENST00000532220.2:n.1192G>A
ENST00000642611.2:n.3529G>A
ENST00000645004.2:n.959G>A
ENST00000682051.1:n.3476G>A
ENST00000682110.1:n.3529G>A
ENST00000682140.1:c.3457G>A	ENSP00000507829.1:p.Ala1153Thr
ENST00000682185.1:n.4765G>A
ENST00000682204.1:c.*1598G>A	ENSP00000507094.1:n.*1598G>A
ENST00000682215.1:n.3526G>A
ENST00000682288.1:c.*1891G>A	ENSP00000507506.1:n.*1891G>A
ENST00000682442.1:n.3749G>A
ENST00000682528.1:n.3606G>A
ENST00000682673.1:n.3473G>A
ENST00000682805.1:n.3526G>A
ENST00000682965.1:c.3396+885G>A	ENSP00000508229.1:n.3396+885G>A
ENST00000683093.1:n.3628G>A
ENST00000683136.1:c.3457G>A	ENSP00000507768.1:p.Ala1153Thr
ENST00000683153.1:n.3685G>A
ENST00000683365.1:n.3631G>A
ENST00000683377.1:n.3529G>A
ENST00000683456.1:c.*597G>A	ENSP00000508318.1:n.*597G>A
ENST00000683522.1:n.3529G>A
ENST00000683562.1:c.*1629G>A	ENSP00000508265.1:n.*1629G>A
ENST00000683693.1:n.3606G>A
ENST00000683725.1:c.3460G>A	ENSP00000507496.1:p.Ala1154Thr
ENST00000684010.1:n.3524G>A
ENST00000684157.1:n.3529G>A
ENST00000684253.1:n.3432G>A
ENST00000684288.1:c.*1632G>A	ENSP00000507143.1:n.*1632G>A
ENST00000684313.1:n.2961G>A
ENST00000684332.1:n.3602G>A
ENST00000684371.1:n.3635G>A
ENST00000684404.1:n.3572G>A
ENST00000684442.1:n.3529G>A
ENST00000684555.1:c.*1672G>A	ENSP00000507705.1:n.*1672G>A
ENST00000684571.1:c.3301G>A	ENSP00000506935.1:p.Ala1101Thr
ENST00000684593.1:c.*3165G>A	ENSP00000507005.1:n.*3165G>A
ENST00000684711.1:c.*1856G>A	ENSP00000506841.1:n.*1856G>A
ENST00000302539.9:c.3463G>A	ENSP00000303960.4:p.Ala1155Thr
ENST00000389817.8:c.3460G>A MANE Select	ENSP00000374467.4:p.Ala1154Thr
ENST00000642271.1:c.3457G>A	ENSP00000493749.1:p.Ala1153Thr
ENST00000642579.1:c.1544G>A
ENST00000642611.1:n.3414G>A
ENST00000642902.1:c.3242G>A
ENST00000643260.1:c.3460G>A	ENSP00000494450.1:p.Ala1154Thr
ENST00000643562.1:c.*1436G>A	ENSP00000496124.1:n.*1436G>A
ENST00000643925.1:c.1584G>A
ENST00000644447.1:c.1816G>A	ENSP00000496282.1:p.Ala606Thr
ENST00000644484.1:c.*1715G>A	ENSP00000493558.1:n.*1715G>A
ENST00000644675.1:c.*1632G>A	ENSP00000494567.1:n.*1632G>A
ENST00000644757.1:c.*1745G>A	ENSP00000495085.1:n.*1745G>A
ENST00000644772.1:c.3526G>A	ENSP00000494321.1:p.Ala1176Thr
ENST00000645004.1:n.599G>A
ENST00000645076.1:c.2659G>A
ENST00000645417.1:c.626G>A
ENST00000645744.1:c.*1724G>A	ENSP00000494564.1:n.*1724G>A
ENST00000645760.1:c.3735G>A
ENST00000645884.1:c.*597G>A	ENSP00000495516.1:n.*597G>A
ENST00000646003.1:c.*1416G>A	ENSP00000495259.1:n.*1416G>A
ENST00000646207.1:c.*1927G>A	ENSP00000495025.1:n.*1927G>A
ENST00000646276.1:c.*1733G>A	ENSP00000496070.1:n.*1733G>A
ENST00000646592.1:c.2766G>A
ENST00000646902.1:c.3457G>A	ENSP00000494101.1:p.Ala1153Thr
ENST00000646993.1:c.*1856G>A	ENSP00000493720.1:n.*1856G>A
ENST00000647013.1:c.3466G>A	ENSP00000496741.1:n.3466G>A
ENST00000647015.1:c.3211G>A	ENSP00000495389.1:p.Ala1071Thr
ENST00000647086.1:c.*3190G>A	ENSP00000493677.1:n.*3190G>A
ENST00000647158.1:c.*1601G>A	ENSP00000495744.1:n.*1601G>A
ENST00000302539.8:c.3463G>A	ENSP00000303960.4:p.Ala1155Thr
ENST00000389817.7:c.3460G>A	ENSP00000374467.3:p.Ala1154Thr
ENST00000524561.1:n.592G>A
ENST00000527905.5:c.*336G>A	ENSP00000431653.1:n.*336G>A
NM_000352.4:c.3460G>A	NP_000343.2:p.Ala1154Thr
NM_001287174.1:c.3463G>A	NP_001274103.1:p.Ala1155Thr
XM_011520331.1:c.3460G>A	XP_011518633.1:p.Ala1154Thr
XM_011520332.1:c.3463G>A	XP_011518634.1:p.Ala1155Thr
XM_011520333.1:c.1960G>A	XP_011518635.1:p.Ala654Thr
XR_930890.1:n.3526G>A
XR_930892.1:n.3426G>A
XR_930893.1:n.3423G>A
NM_001351295.1:c.3526G>A	NP_001338224.1:p.Ala1176Thr
NM_001351296.1:c.3460G>A	NP_001338225.1:p.Ala1154Thr
NM_001351297.1:c.3457G>A	NP_001338226.1:p.Ala1153Thr
NR_147094.1:n.3609G>A
XM_017018197.2:c.3529G>A	XP_016873686.1:p.Ala1177Thr
XM_017018199.1:c.3526G>A	XP_016873688.1:p.Ala1176Thr
XM_017018201.2:c.3529G>A	XP_016873690.1:p.Ala1177Thr
XM_017018202.1:c.2026G>A	XP_016873691.1:p.Ala676Thr
XM_017018204.1:c.1417G>A	XP_016873693.1:p.Ala473Thr
XM_024448668.1:c.1828G>A	XP_024304436.1:p.Ala610Thr
XR_001747945.2:n.3601G>A
XR_001747946.2:n.3532G>A
XR_002957189.1:n.3681G>A
NM_000352.6:c.3460G>A MANE Select	NP_000343.2:p.Ala1154Thr
NM_001287174.2:c.3463G>A	NP_001274103.1:p.Ala1155Thr
NM_001351295.2:c.3526G>A	NP_001338224.1:p.Ala1176Thr
NM_001351296.2:c.3460G>A	NP_001338225.1:p.Ala1154Thr
NM_001351297.2:c.3457G>A	NP_001338226.1:p.Ala1153Thr
NR_147094.2:n.3609G>A
NM_001287174.3:c.3463G>A	NP_001274103.1:p.Ala1155Thr