Canonical Allele Identifier: CA379798552

Gene: ABCC8

Linked Data

• MyVariant Identifiers: chr11:g.17426191A>G (hg19) ; chr11:g.17404644A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17404644A>G , CM000673.2:g.17404644A>G	GRCh38
NC_000011.9:g.17426191A>G , CM000673.1:g.17426191A>G	GRCh37
NC_000011.8:g.17382767A>G	NCBI36
NG_008867.1:g.77259T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524561.2:n.2994T>C
ENST00000528374.2:c.4T>C
ENST00000529967.6:n.1764T>C
ENST00000532220.2:n.1157T>C
ENST00000642611.2:n.3494T>C
ENST00000645004.2:n.924T>C
ENST00000682051.1:n.3441T>C
ENST00000682110.1:n.3494T>C
ENST00000682140.1:c.3422T>C	ENSP00000507829.1:p.Leu1141Pro
ENST00000682185.1:n.4730T>C
ENST00000682204.1:c.*1563T>C	ENSP00000507094.1:n.*1563T>C
ENST00000682215.1:n.3491T>C
ENST00000682288.1:c.*1856T>C	ENSP00000507506.1:n.*1856T>C
ENST00000682442.1:n.3714T>C
ENST00000682528.1:n.3571T>C
ENST00000682673.1:n.3438T>C
ENST00000682805.1:n.3491T>C
ENST00000682965.1:c.3396+850T>C	ENSP00000508229.1:n.3396+850T>C
ENST00000683093.1:n.3593T>C
ENST00000683136.1:c.3422T>C	ENSP00000507768.1:p.Leu1141Pro
ENST00000683153.1:n.3650T>C
ENST00000683365.1:n.3596T>C
ENST00000683377.1:n.3494T>C
ENST00000683456.1:c.*562T>C	ENSP00000508318.1:n.*562T>C
ENST00000683522.1:n.3494T>C
ENST00000683562.1:c.*1594T>C	ENSP00000508265.1:n.*1594T>C
ENST00000683693.1:n.3571T>C
ENST00000683725.1:c.3425T>C	ENSP00000507496.1:p.Leu1142Pro
ENST00000684010.1:n.3489T>C
ENST00000684157.1:n.3494T>C
ENST00000684253.1:n.3397T>C
ENST00000684288.1:c.*1597T>C	ENSP00000507143.1:n.*1597T>C
ENST00000684313.1:n.2926T>C
ENST00000684332.1:n.3567T>C
ENST00000684371.1:n.3600T>C
ENST00000684404.1:n.3537T>C
ENST00000684442.1:n.3494T>C
ENST00000684555.1:c.*1637T>C	ENSP00000507705.1:n.*1637T>C
ENST00000684571.1:c.3266T>C	ENSP00000506935.1:p.Leu1089Pro
ENST00000684593.1:c.*3130T>C	ENSP00000507005.1:n.*3130T>C
ENST00000684711.1:c.*1821T>C	ENSP00000506841.1:n.*1821T>C
ENST00000302539.9:c.3428T>C	ENSP00000303960.4:p.Leu1143Pro
ENST00000389817.8:c.3425T>C MANE Select	ENSP00000374467.4:p.Leu1142Pro
ENST00000642271.1:c.3422T>C	ENSP00000493749.1:p.Leu1141Pro
ENST00000642579.1:c.1509T>C
ENST00000642611.1:n.3379T>C
ENST00000642902.1:c.3207T>C
ENST00000643260.1:c.3425T>C	ENSP00000494450.1:p.Leu1142Pro
ENST00000643562.1:c.*1401T>C	ENSP00000496124.1:n.*1401T>C
ENST00000643925.1:c.1549T>C
ENST00000644447.1:c.1781T>C	ENSP00000496282.1:p.Leu594Pro
ENST00000644484.1:c.*1680T>C	ENSP00000493558.1:n.*1680T>C
ENST00000644675.1:c.*1597T>C	ENSP00000494567.1:n.*1597T>C
ENST00000644757.1:c.*1710T>C	ENSP00000495085.1:n.*1710T>C
ENST00000644772.1:c.3491T>C	ENSP00000494321.1:p.Leu1164Pro
ENST00000645004.1:n.564T>C
ENST00000645076.1:c.2624T>C
ENST00000645417.1:c.591T>C
ENST00000645744.1:c.*1689T>C	ENSP00000494564.1:n.*1689T>C
ENST00000645760.1:c.3700T>C
ENST00000645884.1:c.*562T>C	ENSP00000495516.1:n.*562T>C
ENST00000646003.1:c.*1381T>C	ENSP00000495259.1:n.*1381T>C
ENST00000646207.1:c.*1892T>C	ENSP00000495025.1:n.*1892T>C
ENST00000646276.1:c.*1698T>C	ENSP00000496070.1:n.*1698T>C
ENST00000646592.1:c.2731T>C
ENST00000646902.1:c.3422T>C	ENSP00000494101.1:p.Leu1141Pro
ENST00000646993.1:c.*1821T>C	ENSP00000493720.1:n.*1821T>C
ENST00000647013.1:c.3431T>C	ENSP00000496741.1:n.3431T>C
ENST00000647015.1:c.3176T>C	ENSP00000495389.1:p.Leu1059Pro
ENST00000647086.1:c.*3155T>C	ENSP00000493677.1:n.*3155T>C
ENST00000647158.1:c.*1566T>C	ENSP00000495744.1:n.*1566T>C
ENST00000302539.8:c.3428T>C	ENSP00000303960.4:p.Leu1143Pro
ENST00000389817.7:c.3425T>C	ENSP00000374467.3:p.Leu1142Pro
ENST00000524561.1:n.557T>C
ENST00000527905.5:c.*301T>C	ENSP00000431653.1:n.*301T>C
NM_000352.4:c.3425T>C	NP_000343.2:p.Leu1142Pro
NM_001287174.1:c.3428T>C	NP_001274103.1:p.Leu1143Pro
XM_011520331.1:c.3425T>C	XP_011518633.1:p.Leu1142Pro
XM_011520332.1:c.3428T>C	XP_011518634.1:p.Leu1143Pro
XM_011520333.1:c.1925T>C	XP_011518635.1:p.Leu642Pro
XR_930890.1:n.3491T>C
XR_930892.1:n.3391T>C
XR_930893.1:n.3388T>C
NM_001351295.1:c.3491T>C	NP_001338224.1:p.Leu1164Pro
NM_001351296.1:c.3425T>C	NP_001338225.1:p.Leu1142Pro
NM_001351297.1:c.3422T>C	NP_001338226.1:p.Leu1141Pro
NR_147094.1:n.3574T>C
XM_017018197.2:c.3494T>C	XP_016873686.1:p.Leu1165Pro
XM_017018199.1:c.3491T>C	XP_016873688.1:p.Leu1164Pro
XM_017018201.2:c.3494T>C	XP_016873690.1:p.Leu1165Pro
XM_017018202.1:c.1991T>C	XP_016873691.1:p.Leu664Pro
XM_017018204.1:c.1382T>C	XP_016873693.1:p.Leu461Pro
XM_024448668.1:c.1793T>C	XP_024304436.1:p.Leu598Pro
XR_001747945.2:n.3566T>C
XR_001747946.2:n.3497T>C
XR_002957189.1:n.3646T>C
NM_000352.6:c.3425T>C MANE Select	NP_000343.2:p.Leu1142Pro
NM_001287174.2:c.3428T>C	NP_001274103.1:p.Leu1143Pro
NM_001351295.2:c.3491T>C	NP_001338224.1:p.Leu1164Pro
NM_001351296.2:c.3425T>C	NP_001338225.1:p.Leu1142Pro
NM_001351297.2:c.3422T>C	NP_001338226.1:p.Leu1141Pro
NR_147094.2:n.3574T>C
NM_001287174.3:c.3428T>C	NP_001274103.1:p.Leu1143Pro