Canonical Allele Identifier: CA379806095

Gene: ABCC8

Linked Data

• MyVariant Identifiers: chr11:g.17432093G>T (hg19) ; chr11:g.17410546G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17410546G>T , CM000673.2:g.17410546G>T	GRCh38
NC_000011.9:g.17432093G>T , CM000673.1:g.17432093G>T	GRCh37
NC_000011.8:g.17388669G>T	NCBI36
NG_008867.1:g.71357C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524561.2:n.2333C>A
ENST00000529967.6:n.923C>A
ENST00000642611.2:n.2733C>A
ENST00000682051.1:n.2680C>A
ENST00000682110.1:n.2733C>A
ENST00000682140.1:c.2661C>A	ENSP00000507829.1:p.His887Gln
ENST00000682185.1:n.3969C>A
ENST00000682204.1:c.*802C>A	ENSP00000507094.1:n.*802C>A
ENST00000682215.1:n.2730C>A
ENST00000682288.1:c.*1095C>A	ENSP00000507506.1:n.*1095C>A
ENST00000682442.1:n.2854C>A
ENST00000682528.1:n.2730C>A
ENST00000682673.1:n.2677C>A
ENST00000682805.1:n.2730C>A
ENST00000682965.1:c.2661C>A	ENSP00000508229.1:p.His887Gln
ENST00000683093.1:n.2832C>A
ENST00000683136.1:c.2661C>A	ENSP00000507768.1:p.His887Gln
ENST00000683153.1:n.2889C>A
ENST00000683365.1:n.2835C>A
ENST00000683377.1:n.2733C>A
ENST00000683456.1:c.2664C>A	ENSP00000508318.1:p.His888Gln
ENST00000683522.1:n.2733C>A
ENST00000683562.1:c.*833C>A	ENSP00000508265.1:n.*833C>A
ENST00000683693.1:n.2730C>A
ENST00000683725.1:c.2664C>A	ENSP00000507496.1:p.His888Gln
ENST00000684010.1:n.2648C>A
ENST00000684157.1:n.2733C>A
ENST00000684253.1:n.2636C>A
ENST00000684288.1:c.*836C>A	ENSP00000507143.1:n.*836C>A
ENST00000684313.1:n.2165C>A
ENST00000684332.1:n.2806C>A
ENST00000684371.1:n.2839C>A
ENST00000684404.1:n.2730C>A
ENST00000684442.1:n.2733C>A
ENST00000684555.1:c.*876C>A	ENSP00000507705.1:n.*876C>A
ENST00000684571.1:c.2505C>A	ENSP00000506935.1:p.His835Gln
ENST00000684593.1:c.*2369C>A	ENSP00000507005.1:n.*2369C>A
ENST00000684711.1:c.*1060C>A	ENSP00000506841.1:n.*1060C>A
ENST00000302539.9:c.2667C>A	ENSP00000303960.4:p.His889Gln
ENST00000389817.8:c.2664C>A MANE Select	ENSP00000374467.4:p.His888Gln
ENST00000642271.1:c.2661C>A	ENSP00000493749.1:p.His887Gln
ENST00000642579.1:c.748C>A
ENST00000642611.1:n.2618C>A
ENST00000642902.1:c.2499C>A
ENST00000643260.1:c.2664C>A	ENSP00000494450.1:p.His888Gln
ENST00000643562.1:c.*640C>A	ENSP00000496124.1:n.*640C>A
ENST00000643925.1:c.708C>A
ENST00000644447.1:c.1020C>A	ENSP00000496282.1:p.His340Gln
ENST00000644472.1:c.*1025C>A	ENSP00000495378.1:n.*1025C>A
ENST00000644484.1:c.*873C>A	ENSP00000493558.1:n.*873C>A
ENST00000644542.1:c.*2369C>A	ENSP00000495532.1:n.*2369C>A
ENST00000644675.1:c.*836C>A	ENSP00000494567.1:n.*836C>A
ENST00000644757.1:c.*969C>A	ENSP00000495085.1:n.*969C>A
ENST00000644772.1:c.2730C>A	ENSP00000494321.1:p.His910Gln
ENST00000645076.1:c.1916C>A
ENST00000645744.1:c.*1028C>A	ENSP00000494564.1:n.*1028C>A
ENST00000645760.1:c.2939C>A
ENST00000645884.1:c.2664C>A	ENSP00000495516.1:p.His888Gln
ENST00000646003.1:c.*720C>A	ENSP00000495259.1:n.*720C>A
ENST00000646207.1:c.*1028C>A	ENSP00000495025.1:n.*1028C>A
ENST00000646276.1:c.*937C>A	ENSP00000496070.1:n.*937C>A
ENST00000646592.1:c.1890C>A
ENST00000646902.1:c.2661C>A	ENSP00000494101.1:p.His887Gln
ENST00000646993.1:c.*1060C>A	ENSP00000493720.1:n.*1060C>A
ENST00000647013.1:c.2670C>A	ENSP00000496741.1:n.2670C>A
ENST00000647015.1:c.2415C>A	ENSP00000495389.1:p.His805Gln
ENST00000647086.1:c.*2394C>A	ENSP00000493677.1:n.*2394C>A
ENST00000647158.1:c.*805C>A	ENSP00000495744.1:n.*805C>A
ENST00000302539.8:c.2667C>A	ENSP00000303960.4:p.His889Gln
ENST00000389817.7:c.2664C>A	ENSP00000374467.3:p.His888Gln
ENST00000526921.5:n.348C>A
ENST00000527905.5:c.2634C>A	ENSP00000431653.1:p.His878Gln
ENST00000529967.5:n.333C>A
ENST00000530147.5:n.247C>A
NM_000352.4:c.2664C>A	NP_000343.2:p.His888Gln
NM_001287174.1:c.2667C>A	NP_001274103.1:p.His889Gln
XM_011520331.1:c.2664C>A	XP_011518633.1:p.His888Gln
XM_011520332.1:c.2667C>A	XP_011518634.1:p.His889Gln
XM_011520333.1:c.1164C>A	XP_011518635.1:p.His388Gln
XM_011520334.1:c.2667C>A	XP_011518636.1:p.His889Gln
XR_930890.1:n.2730C>A
XR_930891.1:n.2730C>A
XR_930892.1:n.2730C>A
XR_930893.1:n.2727C>A
NM_001351295.1:c.2730C>A	NP_001338224.1:p.His910Gln
NM_001351296.1:c.2664C>A	NP_001338225.1:p.His888Gln
NM_001351297.1:c.2661C>A	NP_001338226.1:p.His887Gln
NR_147094.1:n.2733C>A
XM_017018197.2:c.2733C>A	XP_016873686.1:p.His911Gln
XM_017018199.1:c.2730C>A	XP_016873688.1:p.His910Gln
XM_017018201.2:c.2733C>A	XP_016873690.1:p.His911Gln
XM_017018202.1:c.1230C>A	XP_016873691.1:p.His410Gln
XM_017018204.1:c.621C>A	XP_016873693.1:p.His207Gln
XM_024448668.1:c.1032C>A	XP_024304436.1:p.His344Gln
XR_001747945.2:n.2805C>A
XR_001747946.2:n.2736C>A
XR_002957189.1:n.2805C>A
NM_000352.6:c.2664C>A MANE Select	NP_000343.2:p.His888Gln
NM_001287174.2:c.2667C>A	NP_001274103.1:p.His889Gln
NM_001351295.2:c.2730C>A	NP_001338224.1:p.His910Gln
NM_001351296.2:c.2664C>A	NP_001338225.1:p.His888Gln
NM_001351297.2:c.2661C>A	NP_001338226.1:p.His887Gln
NR_147094.2:n.2733C>A
NM_001287174.3:c.2667C>A	NP_001274103.1:p.His889Gln