Canonical Allele Identifier: CA1955123631
Gene: ABCC8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17396409G= , CM000673.2:g.17396409G= GRCh38
NC_000011.9:g.17417956G= , CM000673.1:g.17417956G= GRCh37
NC_000011.8:g.17374532G= NCBI36
NG_008867.1:g.85494C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000524561.2:n.3721-479C=
ENST00000528374.2:c.711-479C=
ENST00000529967.6:n.2459-479C=
ENST00000532220.2:n.2874C=
ENST00000642611.2:n.4841C=
ENST00000644057.2:n.563-479C=
ENST00000645004.2:n.1619-479C=
ENST00000682051.1:n.4282-479C=
ENST00000682110.1:n.4335-479C=
ENST00000682140.1:c.3986-479C= ENSP00000507829.1:n.3986-479C=
ENST00000682185.1:n.5425-479C=
ENST00000682204.1:c.*2258-479C= ENSP00000507094.1:n.*2258-479C=
ENST00000682215.1:n.4702-479C=
ENST00000682288.1:c.*2551-479C= ENSP00000507506.1:n.*2551-479C=
ENST00000682442.1:n.4555-479C=
ENST00000682528.1:n.4412-479C=
ENST00000682673.1:n.4279-479C=
ENST00000682805.1:n.4739+469C=
ENST00000682965.1:c.*542-479C= ENSP00000508229.1:n.*542-479C=
ENST00000683093.1:n.4940C=
ENST00000683136.1:c.4003-479C= ENSP00000507768.1:n.4003-479C=
ENST00000683153.1:n.4377-479C=
ENST00000683365.1:n.4437-479C=
ENST00000683377.1:n.4335-479C=
ENST00000683456.1:c.*1257-479C= ENSP00000508318.1:n.*1257-479C=
ENST00000683522.1:n.4335-479C=
ENST00000683562.1:c.*2289-479C= ENSP00000508265.1:n.*2289-479C=
ENST00000683693.1:n.5288C=
ENST00000683725.1:c.4120-479C= ENSP00000507496.1:n.4120-479C=
ENST00000684010.1:n.4330-479C=
ENST00000684157.1:n.4841C=
ENST00000684253.1:n.4238-479C=
ENST00000684288.1:c.*2292-479C= ENSP00000507143.1:n.*2292-479C=
ENST00000684313.1:n.3767-479C=
ENST00000684332.1:n.4408-479C=
ENST00000684371.1:n.4441-479C=
ENST00000684404.1:n.4884C=
ENST00000684442.1:n.4559-479C=
ENST00000684555.1:c.*2332-479C= ENSP00000507705.1:n.*2332-479C=
ENST00000684571.1:c.3961-479C= ENSP00000506935.1:n.3961-479C=
ENST00000684593.1:c.*3825-479C= ENSP00000507005.1:n.*3825-479C=
ENST00000684711.1:c.*2516-479C= ENSP00000506841.1:n.*2516-479C=
ENST00000302539.9:c.4123-479C= ENSP00000303960.4:n.4123-479C=
ENST00000389817.8:c.4120-479C= MANE Select ENSP00000374467.4:n.4120-479C=
ENST00000642271.1:c.4117-479C= ENSP00000493749.1:n.4117-479C=
ENST00000642579.1:c.2174-479C=
ENST00000642611.1:n.4726C=
ENST00000642902.1:c.3902-479C=
ENST00000643260.1:c.4120-479C= ENSP00000494450.1:n.4120-479C=
ENST00000643562.1:c.*2242-479C= ENSP00000496124.1:n.*2242-479C=
ENST00000643925.1:c.2760-479C=
ENST00000644057.1:n.197-479C=
ENST00000644484.1:c.*3027C= ENSP00000493558.1:n.*3027C=
ENST00000644675.1:c.*2292-479C= ENSP00000494567.1:n.*2292-479C=
ENST00000644757.1:c.*3057C= ENSP00000495085.1:n.*3057C=
ENST00000644772.1:c.4186-479C= ENSP00000494321.1:n.4186-479C=
ENST00000645004.1:n.1812+469C=
ENST00000645076.1:c.3319-479C=
ENST00000645417.1:c.1308-479C=
ENST00000645744.1:c.*3406C= ENSP00000494564.1:n.*3406C=
ENST00000645760.1:c.4541-479C=
ENST00000645884.1:c.*1403-479C= ENSP00000495516.1:n.*1403-479C=
ENST00000646003.1:c.*2222-479C= ENSP00000495259.1:n.*2222-479C=
ENST00000646207.1:c.*2957-479C= ENSP00000495025.1:n.*2957-479C=
ENST00000646276.1:c.*3045C= ENSP00000496070.1:n.*3045C=
ENST00000646592.1:c.3426-479C=
ENST00000646902.1:c.4087-479C= ENSP00000494101.1:n.4087-479C=
ENST00000646993.1:c.*2662-479C= ENSP00000493720.1:n.*2662-479C=
ENST00000647013.1:c.4126-479C= ENSP00000496741.1:n.4126-479C=
ENST00000647015.1:c.3871-479C= ENSP00000495389.1:n.3871-479C=
ENST00000647086.1:c.*3706-479C= ENSP00000493677.1:n.*3706-479C=
ENST00000647158.1:c.*2407-479C= ENSP00000495744.1:n.*2407-479C=
ENST00000302539.8:c.4123-479C= ENSP00000303960.4:n.4123-479C=
ENST00000389817.7:c.4120-479C= ENSP00000374467.3:n.4120-479C=
ENST00000528374.1:c.602-479C=
ENST00000532220.1:n.594-479C=
NM_000352.4:c.4120-479C= NP_000343.2:n.4120-479C=
NM_001287174.1:c.4123-479C= NP_001274103.1:n.4123-479C=
XM_011520331.1:c.4120-479C= XP_011518633.1:n.4120-479C=
XM_011520332.1:c.4123-479C= XP_011518634.1:n.4123-479C=
XM_011520333.1:c.2620-479C= XP_011518635.1:n.2620-479C=
XR_930890.1:n.4186-479C=
NM_001351295.1:c.4186-479C= NP_001338224.1:n.4186-479C=
NM_001351296.1:c.4120-479C= NP_001338225.1:n.4120-479C=
NM_001351297.1:c.4117-479C= NP_001338226.1:n.4117-479C=
NR_147094.1:n.4415-479C=
XM_017018197.2:c.4189-479C= XP_016873686.1:n.4189-479C=
XM_017018199.1:c.4186-479C= XP_016873688.1:n.4186-479C=
XM_017018201.2:c.4189-479C= XP_016873690.1:n.4189-479C=
XM_017018202.1:c.2686-479C= XP_016873691.1:n.2686-479C=
XM_017018204.1:c.2077-479C= XP_016873693.1:n.2077-479C=
XM_024448668.1:c.2488-479C= XP_024304436.1:n.2488-479C=
XR_001747945.2:n.4261-479C=
XR_001747946.2:n.4192-479C=
XR_002957189.1:n.5363C=
NM_000352.6:c.4120-479C= MANE Select NP_000343.2:n.4120-479C=
NM_001287174.2:c.4123-479C= NP_001274103.1:n.4123-479C=
NM_001351295.2:c.4186-479C= NP_001338224.1:n.4186-479C=
NM_001351296.2:c.4120-479C= NP_001338225.1:n.4120-479C=
NM_001351297.2:c.4117-479C= NP_001338226.1:n.4117-479C=
NR_147094.2:n.4415-479C=
NM_001287174.3:c.4123-479C= NP_001274103.1:n.4123-479C=