Canonical Allele Identifier: CA379806042
Gene: ABCC8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17410538T>A , CM000673.2:g.17410538T>A GRCh38
NC_000011.9:g.17432085T>A , CM000673.1:g.17432085T>A GRCh37
NC_000011.8:g.17388661T>A NCBI36
NG_008867.1:g.71365A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000524561.2:n.2341A>T
ENST00000529967.6:n.931A>T
ENST00000642611.2:n.2741A>T
ENST00000682051.1:n.2688A>T
ENST00000682110.1:n.2741A>T
ENST00000682140.1:c.2669A>T ENSP00000507829.1:p.Gln890Leu
ENST00000682185.1:n.3977A>T
ENST00000682204.1:c.*810A>T ENSP00000507094.1:n.*810A>T
ENST00000682215.1:n.2738A>T
ENST00000682288.1:c.*1103A>T ENSP00000507506.1:n.*1103A>T
ENST00000682442.1:n.2862A>T
ENST00000682528.1:n.2738A>T
ENST00000682673.1:n.2685A>T
ENST00000682805.1:n.2738A>T
ENST00000682965.1:c.2669A>T ENSP00000508229.1:p.Gln890Leu
ENST00000683093.1:n.2840A>T
ENST00000683136.1:c.2669A>T ENSP00000507768.1:p.Gln890Leu
ENST00000683153.1:n.2897A>T
ENST00000683365.1:n.2843A>T
ENST00000683377.1:n.2741A>T
ENST00000683456.1:c.2672A>T ENSP00000508318.1:p.Gln891Leu
ENST00000683522.1:n.2741A>T
ENST00000683562.1:c.*841A>T ENSP00000508265.1:n.*841A>T
ENST00000683693.1:n.2738A>T
ENST00000683725.1:c.2672A>T ENSP00000507496.1:p.Gln891Leu
ENST00000684010.1:n.2656A>T
ENST00000684157.1:n.2741A>T
ENST00000684253.1:n.2644A>T
ENST00000684288.1:c.*844A>T ENSP00000507143.1:n.*844A>T
ENST00000684313.1:n.2173A>T
ENST00000684332.1:n.2814A>T
ENST00000684371.1:n.2847A>T
ENST00000684404.1:n.2738A>T
ENST00000684442.1:n.2741A>T
ENST00000684555.1:c.*884A>T ENSP00000507705.1:n.*884A>T
ENST00000684571.1:c.2513A>T ENSP00000506935.1:p.Gln838Leu
ENST00000684593.1:c.*2377A>T ENSP00000507005.1:n.*2377A>T
ENST00000684711.1:c.*1068A>T ENSP00000506841.1:n.*1068A>T
ENST00000302539.9:c.2675A>T ENSP00000303960.4:p.Gln892Leu
ENST00000389817.8:c.2672A>T MANE Select ENSP00000374467.4:p.Gln891Leu
ENST00000642271.1:c.2669A>T ENSP00000493749.1:p.Gln890Leu
ENST00000642579.1:c.756A>T
ENST00000642611.1:n.2626A>T
ENST00000642902.1:c.2507A>T
ENST00000643260.1:c.2672A>T ENSP00000494450.1:p.Gln891Leu
ENST00000643562.1:c.*648A>T ENSP00000496124.1:n.*648A>T
ENST00000643925.1:c.716A>T
ENST00000644447.1:c.1028A>T ENSP00000496282.1:p.Gln343Leu
ENST00000644472.1:c.*1033A>T ENSP00000495378.1:n.*1033A>T
ENST00000644484.1:c.*881A>T ENSP00000493558.1:n.*881A>T
ENST00000644542.1:c.*2377A>T ENSP00000495532.1:n.*2377A>T
ENST00000644675.1:c.*844A>T ENSP00000494567.1:n.*844A>T
ENST00000644757.1:c.*977A>T ENSP00000495085.1:n.*977A>T
ENST00000644772.1:c.2738A>T ENSP00000494321.1:p.Gln913Leu
ENST00000645076.1:c.1924A>T
ENST00000645744.1:c.*1036A>T ENSP00000494564.1:n.*1036A>T
ENST00000645760.1:c.2947A>T
ENST00000645884.1:c.2672A>T ENSP00000495516.1:p.Gln891Leu
ENST00000646003.1:c.*728A>T ENSP00000495259.1:n.*728A>T
ENST00000646207.1:c.*1036A>T ENSP00000495025.1:n.*1036A>T
ENST00000646276.1:c.*945A>T ENSP00000496070.1:n.*945A>T
ENST00000646592.1:c.1898A>T
ENST00000646902.1:c.2669A>T ENSP00000494101.1:p.Gln890Leu
ENST00000646993.1:c.*1068A>T ENSP00000493720.1:n.*1068A>T
ENST00000647013.1:c.2678A>T ENSP00000496741.1:n.2678A>T
ENST00000647015.1:c.2423A>T ENSP00000495389.1:p.Gln808Leu
ENST00000647086.1:c.*2402A>T ENSP00000493677.1:n.*2402A>T
ENST00000647158.1:c.*813A>T ENSP00000495744.1:n.*813A>T
ENST00000302539.8:c.2675A>T ENSP00000303960.4:p.Gln892Leu
ENST00000389817.7:c.2672A>T ENSP00000374467.3:p.Gln891Leu
ENST00000526921.5:n.356A>T
ENST00000527905.5:c.2642A>T ENSP00000431653.1:p.Gln881Leu
ENST00000529967.5:n.341A>T
ENST00000530147.5:n.255A>T
NM_000352.4:c.2672A>T NP_000343.2:p.Gln891Leu
NM_001287174.1:c.2675A>T NP_001274103.1:p.Gln892Leu
XM_011520331.1:c.2672A>T XP_011518633.1:p.Gln891Leu
XM_011520332.1:c.2675A>T XP_011518634.1:p.Gln892Leu
XM_011520333.1:c.1172A>T XP_011518635.1:p.Gln391Leu
XM_011520334.1:c.2675A>T XP_011518636.1:p.Gln892Leu
XR_930890.1:n.2738A>T
XR_930891.1:n.2738A>T
XR_930892.1:n.2738A>T
XR_930893.1:n.2735A>T
NM_001351295.1:c.2738A>T NP_001338224.1:p.Gln913Leu
NM_001351296.1:c.2672A>T NP_001338225.1:p.Gln891Leu
NM_001351297.1:c.2669A>T NP_001338226.1:p.Gln890Leu
NR_147094.1:n.2741A>T
XM_017018197.2:c.2741A>T XP_016873686.1:p.Gln914Leu
XM_017018199.1:c.2738A>T XP_016873688.1:p.Gln913Leu
XM_017018201.2:c.2741A>T XP_016873690.1:p.Gln914Leu
XM_017018202.1:c.1238A>T XP_016873691.1:p.Gln413Leu
XM_017018204.1:c.629A>T XP_016873693.1:p.Gln210Leu
XM_024448668.1:c.1040A>T XP_024304436.1:p.Gln347Leu
XR_001747945.2:n.2813A>T
XR_001747946.2:n.2744A>T
XR_002957189.1:n.2813A>T
NM_000352.6:c.2672A>T MANE Select NP_000343.2:p.Gln891Leu
NM_001287174.2:c.2675A>T NP_001274103.1:p.Gln892Leu
NM_001351295.2:c.2738A>T NP_001338224.1:p.Gln913Leu
NM_001351296.2:c.2672A>T NP_001338225.1:p.Gln891Leu
NM_001351297.2:c.2669A>T NP_001338226.1:p.Gln890Leu
NR_147094.2:n.2741A>T
NM_001287174.3:c.2675A>T NP_001274103.1:p.Gln892Leu