Canonical Allele Identifier: CA379806141

Gene: ABCC8

Linked Data

• MyVariant Identifiers: chr11:g.17432101C>T (hg19) ; chr11:g.17410554C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17410554C>T , CM000673.2:g.17410554C>T	GRCh38
NC_000011.9:g.17432101C>T , CM000673.1:g.17432101C>T	GRCh37
NC_000011.8:g.17388677C>T	NCBI36
NG_008867.1:g.71349G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524561.2:n.2325G>A
ENST00000529967.6:n.915G>A
ENST00000642611.2:n.2725G>A
ENST00000682051.1:n.2672G>A
ENST00000682110.1:n.2725G>A
ENST00000682140.1:c.2653G>A	ENSP00000507829.1:p.Val885Met
ENST00000682185.1:n.3961G>A
ENST00000682204.1:c.*794G>A	ENSP00000507094.1:n.*794G>A
ENST00000682215.1:n.2722G>A
ENST00000682288.1:c.*1087G>A	ENSP00000507506.1:n.*1087G>A
ENST00000682442.1:n.2846G>A
ENST00000682528.1:n.2722G>A
ENST00000682673.1:n.2669G>A
ENST00000682805.1:n.2722G>A
ENST00000682965.1:c.2653G>A	ENSP00000508229.1:p.Val885Met
ENST00000683093.1:n.2824G>A
ENST00000683136.1:c.2653G>A	ENSP00000507768.1:p.Val885Met
ENST00000683153.1:n.2881G>A
ENST00000683365.1:n.2827G>A
ENST00000683377.1:n.2725G>A
ENST00000683456.1:c.2656G>A	ENSP00000508318.1:p.Val886Met
ENST00000683522.1:n.2725G>A
ENST00000683562.1:c.*825G>A	ENSP00000508265.1:n.*825G>A
ENST00000683693.1:n.2722G>A
ENST00000683725.1:c.2656G>A	ENSP00000507496.1:p.Val886Met
ENST00000684010.1:n.2640G>A
ENST00000684157.1:n.2725G>A
ENST00000684253.1:n.2628G>A
ENST00000684288.1:c.*828G>A	ENSP00000507143.1:n.*828G>A
ENST00000684313.1:n.2157G>A
ENST00000684332.1:n.2798G>A
ENST00000684371.1:n.2831G>A
ENST00000684404.1:n.2722G>A
ENST00000684442.1:n.2725G>A
ENST00000684555.1:c.*868G>A	ENSP00000507705.1:n.*868G>A
ENST00000684571.1:c.2497G>A	ENSP00000506935.1:p.Val833Met
ENST00000684593.1:c.*2361G>A	ENSP00000507005.1:n.*2361G>A
ENST00000684711.1:c.*1052G>A	ENSP00000506841.1:n.*1052G>A
ENST00000302539.9:c.2659G>A	ENSP00000303960.4:p.Val887Met
ENST00000389817.8:c.2656G>A MANE Select	ENSP00000374467.4:p.Val886Met
ENST00000642271.1:c.2653G>A	ENSP00000493749.1:p.Val885Met
ENST00000642579.1:c.740G>A
ENST00000642611.1:n.2610G>A
ENST00000642902.1:c.2491G>A
ENST00000643260.1:c.2656G>A	ENSP00000494450.1:p.Val886Met
ENST00000643562.1:c.*632G>A	ENSP00000496124.1:n.*632G>A
ENST00000643925.1:c.700G>A
ENST00000644447.1:c.1012G>A	ENSP00000496282.1:p.Val338Met
ENST00000644472.1:c.*1017G>A	ENSP00000495378.1:n.*1017G>A
ENST00000644484.1:c.*865G>A	ENSP00000493558.1:n.*865G>A
ENST00000644542.1:c.*2361G>A	ENSP00000495532.1:n.*2361G>A
ENST00000644675.1:c.*828G>A	ENSP00000494567.1:n.*828G>A
ENST00000644757.1:c.*961G>A	ENSP00000495085.1:n.*961G>A
ENST00000644772.1:c.2722G>A	ENSP00000494321.1:p.Val908Met
ENST00000645076.1:c.1908G>A
ENST00000645744.1:c.*1020G>A	ENSP00000494564.1:n.*1020G>A
ENST00000645760.1:c.2931G>A
ENST00000645884.1:c.2656G>A	ENSP00000495516.1:p.Val886Met
ENST00000646003.1:c.*712G>A	ENSP00000495259.1:n.*712G>A
ENST00000646207.1:c.*1020G>A	ENSP00000495025.1:n.*1020G>A
ENST00000646276.1:c.*929G>A	ENSP00000496070.1:n.*929G>A
ENST00000646592.1:c.1882G>A
ENST00000646902.1:c.2653G>A	ENSP00000494101.1:p.Val885Met
ENST00000646993.1:c.*1052G>A	ENSP00000493720.1:n.*1052G>A
ENST00000647013.1:c.2662G>A	ENSP00000496741.1:n.2662G>A
ENST00000647015.1:c.2407G>A	ENSP00000495389.1:p.Val803Met
ENST00000647086.1:c.*2386G>A	ENSP00000493677.1:n.*2386G>A
ENST00000647158.1:c.*797G>A	ENSP00000495744.1:n.*797G>A
ENST00000302539.8:c.2659G>A	ENSP00000303960.4:p.Val887Met
ENST00000389817.7:c.2656G>A	ENSP00000374467.3:p.Val886Met
ENST00000526921.5:n.340G>A
ENST00000527905.5:c.2626G>A	ENSP00000431653.1:p.Val876Met
ENST00000529967.5:n.325G>A
ENST00000530147.5:n.239G>A
NM_000352.4:c.2656G>A	NP_000343.2:p.Val886Met
NM_001287174.1:c.2659G>A	NP_001274103.1:p.Val887Met
XM_011520331.1:c.2656G>A	XP_011518633.1:p.Val886Met
XM_011520332.1:c.2659G>A	XP_011518634.1:p.Val887Met
XM_011520333.1:c.1156G>A	XP_011518635.1:p.Val386Met
XM_011520334.1:c.2659G>A	XP_011518636.1:p.Val887Met
XR_930890.1:n.2722G>A
XR_930891.1:n.2722G>A
XR_930892.1:n.2722G>A
XR_930893.1:n.2719G>A
NM_001351295.1:c.2722G>A	NP_001338224.1:p.Val908Met
NM_001351296.1:c.2656G>A	NP_001338225.1:p.Val886Met
NM_001351297.1:c.2653G>A	NP_001338226.1:p.Val885Met
NR_147094.1:n.2725G>A
XM_017018197.2:c.2725G>A	XP_016873686.1:p.Val909Met
XM_017018199.1:c.2722G>A	XP_016873688.1:p.Val908Met
XM_017018201.2:c.2725G>A	XP_016873690.1:p.Val909Met
XM_017018202.1:c.1222G>A	XP_016873691.1:p.Val408Met
XM_017018204.1:c.613G>A	XP_016873693.1:p.Val205Met
XM_024448668.1:c.1024G>A	XP_024304436.1:p.Val342Met
XR_001747945.2:n.2797G>A
XR_001747946.2:n.2728G>A
XR_002957189.1:n.2797G>A
NM_000352.6:c.2656G>A MANE Select	NP_000343.2:p.Val886Met
NM_001287174.2:c.2659G>A	NP_001274103.1:p.Val887Met
NM_001351295.2:c.2722G>A	NP_001338224.1:p.Val908Met
NM_001351296.2:c.2656G>A	NP_001338225.1:p.Val886Met
NM_001351297.2:c.2653G>A	NP_001338226.1:p.Val885Met
NR_147094.2:n.2725G>A
NM_001287174.3:c.2659G>A	NP_001274103.1:p.Val887Met