Canonical Allele Identifier: CA2697548446

Gene: ABCC8

Linked Data

• ClinVar Variation Id: 2744740
• ClinVar RCV Id: RCV003565769

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17428276del , CM000673.2:g.17428276del	GRCh38
NC_000011.9:g.17449823del , CM000673.1:g.17449823del	GRCh37
NC_000011.8:g.17406399del	NCBI36
NG_008867.1:g.53627del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524561.2:n.1709+13del
ENST00000529967.6:n.299+13del
ENST00000642611.2:n.2106+13del
ENST00000682051.1:n.2053+13del
ENST00000682110.1:n.2106+13del
ENST00000682140.1:c.2037+13del	ENSP00000507829.1:n.2037+13del
ENST00000682185.1:n.3345+13del
ENST00000682204.1:c.*178+13del	ENSP00000507094.1:n.*178+13del
ENST00000682215.1:n.2106+13del
ENST00000682288.1:c.*468+13del	ENSP00000507506.1:n.*468+13del
ENST00000682442.1:n.2227+13del
ENST00000682528.1:n.2106+13del
ENST00000682673.1:n.2053+13del
ENST00000682805.1:n.2106+13del
ENST00000682965.1:c.2037+13del	ENSP00000508229.1:n.2037+13del
ENST00000683093.1:n.2208+13del
ENST00000683136.1:c.2037+13del	ENSP00000507768.1:n.2037+13del
ENST00000683153.1:n.2265+13del
ENST00000683253.1:n.3122+13del
ENST00000683365.1:n.2208+13del
ENST00000683377.1:n.2106+13del
ENST00000683456.1:c.2037+13del	ENSP00000508318.1:n.2037+13del
ENST00000683522.1:n.2106+13del
ENST00000683562.1:c.*209+13del	ENSP00000508265.1:n.*209+13del
ENST00000683693.1:n.2106+13del
ENST00000683725.1:c.2040+13del	ENSP00000507496.1:n.2040+13del
ENST00000684010.1:n.2106+13del
ENST00000684157.1:n.2106+13del
ENST00000684253.1:n.2012+13del
ENST00000684288.1:c.*209+13del	ENSP00000507143.1:n.*209+13del
ENST00000684313.1:n.1724-11314del
ENST00000684332.1:n.2179+13del
ENST00000684371.1:n.2212+13del
ENST00000684404.1:n.2106+13del
ENST00000684442.1:n.2106+13del
ENST00000684555.1:c.*249+13del	ENSP00000507705.1:n.*249+13del
ENST00000684571.1:c.1881+13del	ENSP00000506935.1:n.1881+13del
ENST00000684593.1:c.*1745+13del	ENSP00000507005.1:n.*1745+13del
ENST00000684711.1:c.*436+13del	ENSP00000506841.1:n.*436+13del
ENST00000302539.9:c.2040+13del	ENSP00000303960.4:n.2040+13del
ENST00000389817.8:c.2040+13del MANE Select	ENSP00000374467.4:n.2040+13del
ENST00000532728.6:c.1621+13del
ENST00000642271.1:c.2037+13del	ENSP00000493749.1:n.2037+13del
ENST00000642579.1:c.121+13del
ENST00000642611.1:n.1991+13del
ENST00000642902.1:c.1875+13del
ENST00000643260.1:c.2037+13del	ENSP00000494450.1:n.2037+13del
ENST00000643562.1:c.*16+13del	ENSP00000496124.1:n.*16+13del
ENST00000644447.1:c.393+13del	ENSP00000496282.1:n.393+13del
ENST00000644472.1:c.*401+13del	ENSP00000495378.1:n.*401+13del
ENST00000644484.1:c.*249+13del	ENSP00000493558.1:n.*249+13del
ENST00000644542.1:c.*1742+13del	ENSP00000495532.1:n.*1742+13del
ENST00000644649.1:c.1210+13del
ENST00000644675.1:c.*209+13del	ENSP00000494567.1:n.*209+13del
ENST00000644757.1:c.*342+13del	ENSP00000495085.1:n.*342+13del
ENST00000644772.1:c.2106+13del	ENSP00000494321.1:n.2106+13del
ENST00000645076.1:c.1292+13del
ENST00000645744.1:c.*401+13del	ENSP00000494564.1:n.*401+13del
ENST00000645760.1:c.2315+13del
ENST00000645884.1:c.2037+13del	ENSP00000495516.1:n.2037+13del
ENST00000646003.1:c.*178+13del	ENSP00000495259.1:n.*178+13del
ENST00000646207.1:c.*401+13del	ENSP00000495025.1:n.*401+13del
ENST00000646276.1:c.*310+13del	ENSP00000496070.1:n.*310+13del
ENST00000646592.1:c.1263+13del
ENST00000646902.1:c.2037+13del	ENSP00000494101.1:n.2037+13del
ENST00000646993.1:c.*436+13del	ENSP00000493720.1:n.*436+13del
ENST00000647013.1:c.2043+13del	ENSP00000496741.1:n.2043+13del
ENST00000647015.1:c.1788+13del	ENSP00000495389.1:n.1788+13del
ENST00000647086.1:c.*1767+13del	ENSP00000493677.1:n.*1767+13del
ENST00000647158.1:c.*178+13del	ENSP00000495744.1:n.*178+13del
ENST00000302539.8:c.2040+13del	ENSP00000303960.4:n.2040+13del
ENST00000389817.7:c.2040+13del	ENSP00000374467.3:n.2040+13del
ENST00000527905.5:c.2010+13del	ENSP00000431653.1:n.2010+13del
NM_000352.4:c.2040+13del	NP_000343.2:n.2040+13del
NM_001287174.1:c.2040+13del	NP_001274103.1:n.2040+13del
XM_011520331.1:c.2037+13del	XP_011518633.1:n.2037+13del
XM_011520332.1:c.2040+13del	XP_011518634.1:n.2040+13del
XM_011520333.1:c.537+13del	XP_011518635.1:n.537+13del
XM_011520334.1:c.2040+13del	XP_011518636.1:n.2040+13del
XR_930890.1:n.2103+13del
XR_930891.1:n.2103+13del
XR_930892.1:n.2103+13del
XR_930893.1:n.2103+13del
NM_001351295.1:c.2106+13del	NP_001338224.1:n.2106+13del
NM_001351296.1:c.2037+13del	NP_001338225.1:n.2037+13del
NM_001351297.1:c.2037+13del	NP_001338226.1:n.2037+13del
NR_147094.1:n.2106+13del
XM_017018197.2:c.2106+13del	XP_016873686.1:n.2106+13del
XM_017018199.1:c.2103+13del	XP_016873688.1:n.2103+13del
XM_017018201.2:c.2106+13del	XP_016873690.1:n.2106+13del
XM_017018202.1:c.603+13del	XP_016873691.1:n.603+13del
XM_017018204.1:c.-4+13del	XP_016873693.1:n.-4+13del
XM_024448668.1:c.405+13del	XP_024304436.1:n.405+13del
XR_001747945.2:n.2178+13del
XR_001747946.2:n.2112+13del
XR_002957189.1:n.2178+13del
NM_000352.6:c.2040+13del MANE Select	NP_000343.2:n.2040+13del
NM_001287174.2:c.2040+13del	NP_001274103.1:n.2040+13del
NM_001351295.2:c.2106+13del	NP_001338224.1:n.2106+13del
NM_001351296.2:c.2037+13del	NP_001338225.1:n.2037+13del
NM_001351297.2:c.2037+13del	NP_001338226.1:n.2037+13del
NR_147094.2:n.2106+13del
NM_001287174.3:c.2040+13del	NP_001274103.1:n.2040+13del