Canonical Allele Identifier: CA379787419

Gene: ABCC8

Linked Data

• MyVariant Identifiers: chr11:g.17417257T>A (hg19) ; chr11:g.17395710T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17395710T>A , CM000673.2:g.17395710T>A	GRCh38
NC_000011.9:g.17417257T>A , CM000673.1:g.17417257T>A	GRCh37
NC_000011.8:g.17373833T>A	NCBI36
NG_008867.1:g.86193A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524561.2:n.3808A>T
ENST00000528374.2:c.798A>T
ENST00000529967.6:n.2546A>T
ENST00000532220.2:n.3440A>T
ENST00000642611.2:n.5540A>T
ENST00000644057.2:n.783A>T
ENST00000645004.2:n.1706A>T
ENST00000682051.1:n.4369A>T
ENST00000682110.1:n.4422A>T
ENST00000682140.1:c.4073A>T	ENSP00000507829.1:p.His1358Leu
ENST00000682185.1:n.5512A>T
ENST00000682204.1:c.*2345A>T	ENSP00000507094.1:n.*2345A>T
ENST00000682215.1:n.4789A>T
ENST00000682288.1:c.*2638A>T	ENSP00000507506.1:n.*2638A>T
ENST00000682442.1:n.4642A>T
ENST00000682528.1:n.4499A>T
ENST00000682673.1:n.4366A>T
ENST00000682805.1:n.4827A>T
ENST00000682965.1:c.*629A>T	ENSP00000508229.1:n.*629A>T
ENST00000683093.1:n.5506A>T
ENST00000683136.1:c.4090A>T	ENSP00000507768.1:p.Ile1364Phe
ENST00000683153.1:n.4464A>T
ENST00000683365.1:n.4524A>T
ENST00000683377.1:n.4422A>T
ENST00000683456.1:c.*1344A>T	ENSP00000508318.1:n.*1344A>T
ENST00000683522.1:n.4422A>T
ENST00000683562.1:c.*2376A>T	ENSP00000508265.1:n.*2376A>T
ENST00000683693.1:n.5987A>T
ENST00000683725.1:c.4207A>T	ENSP00000507496.1:p.Ile1403Phe
ENST00000684010.1:n.4417A>T
ENST00000684157.1:n.5407A>T
ENST00000684253.1:n.4325A>T
ENST00000684288.1:c.*2379A>T	ENSP00000507143.1:n.*2379A>T
ENST00000684313.1:n.3854A>T
ENST00000684332.1:n.4495A>T
ENST00000684371.1:n.4528A>T
ENST00000684404.1:n.5450A>T
ENST00000684442.1:n.4646A>T
ENST00000684555.1:c.*2419A>T	ENSP00000507705.1:n.*2419A>T
ENST00000684571.1:c.4048A>T	ENSP00000506935.1:p.Ile1350Phe
ENST00000684593.1:c.*3912A>T	ENSP00000507005.1:n.*3912A>T
ENST00000684711.1:c.*2603A>T	ENSP00000506841.1:n.*2603A>T
ENST00000302539.9:c.4210A>T	ENSP00000303960.4:p.Ile1404Phe
ENST00000389817.8:c.4207A>T MANE Select	ENSP00000374467.4:p.Ile1403Phe
ENST00000642271.1:c.4204A>T	ENSP00000493749.1:p.Ile1402Phe
ENST00000642579.1:c.2261A>T
ENST00000642611.1:n.5425A>T
ENST00000642902.1:c.3989A>T
ENST00000643260.1:c.4207A>T	ENSP00000494450.1:p.Ile1403Phe
ENST00000643562.1:c.*2329A>T	ENSP00000496124.1:n.*2329A>T
ENST00000643925.1:c.2847A>T
ENST00000644057.1:n.284A>T
ENST00000644484.1:c.*3593A>T	ENSP00000493558.1:n.*3593A>T
ENST00000644675.1:c.*2379A>T	ENSP00000494567.1:n.*2379A>T
ENST00000644757.1:c.*3202+554A>T	ENSP00000495085.1:n.*3202+554A>T
ENST00000644772.1:c.4273A>T	ENSP00000494321.1:p.Ile1425Phe
ENST00000645004.1:n.1900A>T
ENST00000645076.1:c.3406A>T
ENST00000645417.1:c.1395A>T
ENST00000645744.1:c.*3964-72A>T	ENSP00000494564.1:n.*3964-72A>T
ENST00000645760.1:c.4628A>T
ENST00000645884.1:c.*1490A>T	ENSP00000495516.1:n.*1490A>T
ENST00000646003.1:c.*2301-72A>T	ENSP00000495259.1:n.*2301-72A>T
ENST00000646207.1:c.*3044A>T	ENSP00000495025.1:n.*3044A>T
ENST00000646276.1:c.*3611A>T	ENSP00000496070.1:n.*3611A>T
ENST00000646592.1:c.3513A>T
ENST00000646902.1:c.4174A>T	ENSP00000494101.1:p.Ile1392Phe
ENST00000646993.1:c.*2749A>T	ENSP00000493720.1:n.*2749A>T
ENST00000647013.1:c.4213A>T	ENSP00000496741.1:n.4213A>T
ENST00000647015.1:c.3958A>T	ENSP00000495389.1:p.Ile1320Phe
ENST00000647086.1:c.*3793A>T	ENSP00000493677.1:n.*3793A>T
ENST00000647158.1:c.*2494A>T	ENSP00000495744.1:n.*2494A>T
ENST00000302539.8:c.4210A>T	ENSP00000303960.4:p.Ile1404Phe
ENST00000389817.7:c.4207A>T	ENSP00000374467.3:p.Ile1403Phe
ENST00000525022.1:n.206A>T
ENST00000526037.5:n.71A>T
ENST00000526168.5:c.67-72A>T
ENST00000531642.5:c.43A>T
NM_000352.4:c.4207A>T	NP_000343.2:p.Ile1403Phe
NM_001287174.1:c.4210A>T	NP_001274103.1:p.Ile1404Phe
XM_011520331.1:c.4207A>T	XP_011518633.1:p.Ile1403Phe
XM_011520332.1:c.4210A>T	XP_011518634.1:p.Ile1404Phe
XM_011520333.1:c.2707A>T	XP_011518635.1:p.Ile903Phe
XR_930890.1:n.4273A>T
NM_001351295.1:c.4273A>T	NP_001338224.1:p.Ile1425Phe
NM_001351296.1:c.4207A>T	NP_001338225.1:p.Ile1403Phe
NM_001351297.1:c.4204A>T	NP_001338226.1:p.Ile1402Phe
NR_147094.1:n.4502A>T
XM_017018197.2:c.4276A>T	XP_016873686.1:p.Ile1426Phe
XM_017018199.1:c.4273A>T	XP_016873688.1:p.Ile1425Phe
XM_017018201.2:c.4276A>T	XP_016873690.1:p.Ile1426Phe
XM_017018202.1:c.2773A>T	XP_016873691.1:p.Ile925Phe
XM_017018204.1:c.2164A>T	XP_016873693.1:p.Ile722Phe
XM_024448668.1:c.2575A>T	XP_024304436.1:p.Ile859Phe
XR_001747945.2:n.4348A>T
XR_001747946.2:n.4279A>T
XR_002957189.1:n.6062A>T
NM_000352.6:c.4207A>T MANE Select	NP_000343.2:p.Ile1403Phe
NM_001287174.2:c.4210A>T	NP_001274103.1:p.Ile1404Phe
NM_001351295.2:c.4273A>T	NP_001338224.1:p.Ile1425Phe
NM_001351296.2:c.4207A>T	NP_001338225.1:p.Ile1403Phe
NM_001351297.2:c.4204A>T	NP_001338226.1:p.Ile1402Phe
NR_147094.2:n.4502A>T
NM_001287174.3:c.4210A>T	NP_001274103.1:p.Ile1404Phe