Canonical Allele Identifier: CA379803013

Gene: ABCC8

Linked Data

• MyVariant Identifiers: chr11:g.17428331C>G (hg19) ; chr11:g.17406784C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17406784C>G , CM000673.2:g.17406784C>G	GRCh38
NC_000011.9:g.17428331C>G , CM000673.1:g.17428331C>G	GRCh37
NC_000011.8:g.17384907C>G	NCBI36
NG_008867.1:g.75119G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524561.2:n.2736G>C
ENST00000529967.6:n.1506G>C
ENST00000532220.2:n.899G>C
ENST00000642611.2:n.3236G>C
ENST00000645004.2:n.666G>C
ENST00000682051.1:n.3183G>C
ENST00000682110.1:n.3236G>C
ENST00000682140.1:c.3164G>C	ENSP00000507829.1:p.Cys1055Ser
ENST00000682185.1:n.4472G>C
ENST00000682204.1:c.*1305G>C	ENSP00000507094.1:n.*1305G>C
ENST00000682215.1:n.3233G>C
ENST00000682288.1:c.*1598G>C	ENSP00000507506.1:n.*1598G>C
ENST00000682442.1:n.3456G>C
ENST00000682528.1:n.3313G>C
ENST00000682673.1:n.3180G>C
ENST00000682805.1:n.3233G>C
ENST00000682965.1:c.3164G>C	ENSP00000508229.1:p.Cys1055Ser
ENST00000683093.1:n.3335G>C
ENST00000683136.1:c.3164G>C	ENSP00000507768.1:p.Cys1055Ser
ENST00000683153.1:n.3392G>C
ENST00000683365.1:n.3338G>C
ENST00000683377.1:n.3236G>C
ENST00000683456.1:c.*304G>C	ENSP00000508318.1:n.*304G>C
ENST00000683522.1:n.3236G>C
ENST00000683562.1:c.*1336G>C	ENSP00000508265.1:n.*1336G>C
ENST00000683693.1:n.3313G>C
ENST00000683725.1:c.3167G>C	ENSP00000507496.1:p.Cys1056Ser
ENST00000684010.1:n.3231G>C
ENST00000684157.1:n.3236G>C
ENST00000684253.1:n.3139G>C
ENST00000684288.1:c.*1339G>C	ENSP00000507143.1:n.*1339G>C
ENST00000684313.1:n.2668G>C
ENST00000684332.1:n.3309G>C
ENST00000684371.1:n.3342G>C
ENST00000684404.1:n.3279G>C
ENST00000684442.1:n.3236G>C
ENST00000684555.1:c.*1379G>C	ENSP00000507705.1:n.*1379G>C
ENST00000684571.1:c.3008G>C	ENSP00000506935.1:p.Cys1003Ser
ENST00000684593.1:c.*2872G>C	ENSP00000507005.1:n.*2872G>C
ENST00000684711.1:c.*1563G>C	ENSP00000506841.1:n.*1563G>C
ENST00000302539.9:c.3170G>C	ENSP00000303960.4:p.Cys1057Ser
ENST00000389817.8:c.3167G>C MANE Select	ENSP00000374467.4:p.Cys1056Ser
ENST00000642271.1:c.3164G>C	ENSP00000493749.1:p.Cys1055Ser
ENST00000642579.1:c.1251G>C
ENST00000642611.1:n.3121G>C
ENST00000642902.1:c.2949G>C
ENST00000643260.1:c.3167G>C	ENSP00000494450.1:p.Cys1056Ser
ENST00000643562.1:c.*1143G>C	ENSP00000496124.1:n.*1143G>C
ENST00000643925.1:c.1291G>C
ENST00000644447.1:c.1523G>C	ENSP00000496282.1:p.Cys508Ser
ENST00000644484.1:c.*1422G>C	ENSP00000493558.1:n.*1422G>C
ENST00000644542.1:c.*2971G>C	ENSP00000495532.1:n.*2971G>C
ENST00000644675.1:c.*1339G>C	ENSP00000494567.1:n.*1339G>C
ENST00000644757.1:c.*1452G>C	ENSP00000495085.1:n.*1452G>C
ENST00000644772.1:c.3233G>C	ENSP00000494321.1:p.Cys1078Ser
ENST00000645004.1:n.306G>C
ENST00000645076.1:c.2366G>C
ENST00000645417.1:c.333G>C
ENST00000645744.1:c.*1431G>C	ENSP00000494564.1:n.*1431G>C
ENST00000645760.1:c.3442G>C
ENST00000645884.1:c.*304G>C	ENSP00000495516.1:n.*304G>C
ENST00000646003.1:c.*1123G>C	ENSP00000495259.1:n.*1123G>C
ENST00000646207.1:c.*1634G>C	ENSP00000495025.1:n.*1634G>C
ENST00000646276.1:c.*1440G>C	ENSP00000496070.1:n.*1440G>C
ENST00000646592.1:c.2473G>C
ENST00000646902.1:c.3164G>C	ENSP00000494101.1:p.Cys1055Ser
ENST00000646993.1:c.*1563G>C	ENSP00000493720.1:n.*1563G>C
ENST00000647013.1:c.3173G>C	ENSP00000496741.1:n.3173G>C
ENST00000647015.1:c.2918G>C	ENSP00000495389.1:p.Cys973Ser
ENST00000647086.1:c.*2897G>C	ENSP00000493677.1:n.*2897G>C
ENST00000647158.1:c.*1308G>C	ENSP00000495744.1:n.*1308G>C
ENST00000302539.8:c.3170G>C	ENSP00000303960.4:p.Cys1057Ser
ENST00000389817.7:c.3167G>C	ENSP00000374467.3:p.Cys1056Ser
ENST00000524561.1:n.299G>C
ENST00000526921.5:n.851G>C
ENST00000527905.5:c.*43G>C	ENSP00000431653.1:n.*43G>C
NM_000352.4:c.3167G>C	NP_000343.2:p.Cys1056Ser
NM_001287174.1:c.3170G>C	NP_001274103.1:p.Cys1057Ser
XM_011520331.1:c.3167G>C	XP_011518633.1:p.Cys1056Ser
XM_011520332.1:c.3170G>C	XP_011518634.1:p.Cys1057Ser
XM_011520333.1:c.1667G>C	XP_011518635.1:p.Cys556Ser
XR_930890.1:n.3233G>C
XR_930891.1:n.3233G>C
XR_930892.1:n.3133G>C
XR_930893.1:n.3130G>C
NM_001351295.1:c.3233G>C	NP_001338224.1:p.Cys1078Ser
NM_001351296.1:c.3167G>C	NP_001338225.1:p.Cys1056Ser
NM_001351297.1:c.3164G>C	NP_001338226.1:p.Cys1055Ser
NR_147094.1:n.3316G>C
XM_017018197.2:c.3236G>C	XP_016873686.1:p.Cys1079Ser
XM_017018199.1:c.3233G>C	XP_016873688.1:p.Cys1078Ser
XM_017018201.2:c.3236G>C	XP_016873690.1:p.Cys1079Ser
XM_017018202.1:c.1733G>C	XP_016873691.1:p.Cys578Ser
XM_017018204.1:c.1124G>C	XP_016873693.1:p.Cys375Ser
XM_024448668.1:c.1535G>C	XP_024304436.1:p.Cys512Ser
XR_001747945.2:n.3308G>C
XR_001747946.2:n.3239G>C
XR_002957189.1:n.3388G>C
NM_000352.6:c.3167G>C MANE Select	NP_000343.2:p.Cys1056Ser
NM_001287174.2:c.3170G>C	NP_001274103.1:p.Cys1057Ser
NM_001351295.2:c.3233G>C	NP_001338224.1:p.Cys1078Ser
NM_001351296.2:c.3167G>C	NP_001338225.1:p.Cys1056Ser
NM_001351297.2:c.3164G>C	NP_001338226.1:p.Cys1055Ser
NR_147094.2:n.3316G>C
NM_001287174.3:c.3170G>C	NP_001274103.1:p.Cys1057Ser