Canonical Allele Identifier: CA379817163

Gene: ABCC8

Linked Data

• gnomAD v4: 11-17430950-C-G
• MyVariant Identifiers: chr11:g.17452497C>G (hg19) ; chr11:g.17430950C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17430950C>G , CM000673.2:g.17430950C>G	GRCh38
NC_000011.9:g.17452497C>G , CM000673.1:g.17452497C>G	GRCh37
NC_000011.8:g.17409073C>G	NCBI36
NG_008867.1:g.50953G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000524561.2:n.1318G>C
ENST00000526002.2:n.1708G>C
ENST00000528202.6:n.1820G>C
ENST00000642611.2:n.1747G>C
ENST00000682051.1:n.1694G>C
ENST00000682110.1:n.1747G>C
ENST00000682140.1:c.1678G>C	ENSP00000507829.1:p.Gly560Arg
ENST00000682185.1:n.2986G>C
ENST00000682204.1:c.1668+1254G>C	ENSP00000507094.1:n.1668+1254G>C
ENST00000682215.1:n.1747G>C
ENST00000682288.1:c.*77G>C	ENSP00000507506.1:n.*77G>C
ENST00000682442.1:n.1868G>C
ENST00000682528.1:n.1747G>C
ENST00000682673.1:n.1694G>C
ENST00000682805.1:n.1747G>C
ENST00000682965.1:c.1678G>C	ENSP00000508229.1:p.Gly560Arg
ENST00000683093.1:n.1849G>C
ENST00000683136.1:c.1678G>C	ENSP00000507768.1:p.Gly560Arg
ENST00000683153.1:n.1747G>C
ENST00000683253.1:n.2763G>C
ENST00000683365.1:n.1849G>C
ENST00000683377.1:n.1747G>C
ENST00000683456.1:c.1678G>C	ENSP00000508318.1:p.Gly560Arg
ENST00000683522.1:n.1747G>C
ENST00000683531.1:n.1750G>C
ENST00000683562.1:c.1681G>C	ENSP00000508265.1:p.Gly561Arg
ENST00000683693.1:n.1747G>C
ENST00000683725.1:c.1681G>C	ENSP00000507496.1:p.Gly561Arg
ENST00000684010.1:n.1747G>C
ENST00000684157.1:n.1747G>C
ENST00000684253.1:n.1789+1254G>C
ENST00000684288.1:c.1681G>C	ENSP00000507143.1:p.Gly561Arg
ENST00000684313.1:n.1723+11770G>C
ENST00000684332.1:n.1820G>C
ENST00000684371.1:n.1694G>C
ENST00000684404.1:n.1747G>C
ENST00000684442.1:n.1747G>C
ENST00000684555.1:c.1671+1254G>C	ENSP00000507705.1:n.1671+1254G>C
ENST00000684571.1:c.1522G>C	ENSP00000506935.1:p.Gly508Arg
ENST00000684593.1:c.*1386G>C	ENSP00000507005.1:n.*1386G>C
ENST00000684711.1:c.*77G>C	ENSP00000506841.1:n.*77G>C
ENST00000302539.9:c.1681G>C	ENSP00000303960.4:p.Gly561Arg
ENST00000389817.8:c.1681G>C MANE Select	ENSP00000374467.4:p.Gly561Arg
ENST00000532728.6:c.1398+1254G>C
ENST00000635881.1:n.1709G>C
ENST00000642271.1:c.1678G>C	ENSP00000493749.1:p.Gly560Arg
ENST00000642611.1:n.1632G>C
ENST00000642902.1:c.1652+1254G>C
ENST00000643260.1:c.1678G>C	ENSP00000494450.1:p.Gly560Arg
ENST00000643562.1:c.1681G>C	ENSP00000496124.1:p.Gly561Arg
ENST00000644447.1:c.34G>C	ENSP00000496282.1:p.Gly12Arg
ENST00000644472.1:c.*42G>C	ENSP00000495378.1:n.*42G>C
ENST00000644484.1:c.1668+1254G>C	ENSP00000493558.1:n.1668+1254G>C
ENST00000644542.1:c.*1383G>C	ENSP00000495532.1:n.*1383G>C
ENST00000644649.1:c.851G>C
ENST00000644675.1:c.1678G>C	ENSP00000494567.1:p.Gly560Arg
ENST00000644757.1:c.*87+1254G>C	ENSP00000495085.1:n.*87+1254G>C
ENST00000644772.1:c.1681G>C	ENSP00000494321.1:p.Gly561Arg
ENST00000645076.1:c.963G>C
ENST00000645744.1:c.*42G>C	ENSP00000494564.1:n.*42G>C
ENST00000645760.1:c.1956G>C
ENST00000645884.1:c.1678G>C	ENSP00000495516.1:p.Gly560Arg
ENST00000646003.1:c.1668+1254G>C	ENSP00000495259.1:n.1668+1254G>C
ENST00000646207.1:c.*42G>C	ENSP00000495025.1:n.*42G>C
ENST00000646276.1:c.*87+1254G>C	ENSP00000496070.1:n.*87+1254G>C
ENST00000646592.1:c.882-2280G>C
ENST00000646902.1:c.1678G>C	ENSP00000494101.1:p.Gly560Arg
ENST00000646993.1:c.*77G>C	ENSP00000493720.1:n.*77G>C
ENST00000647013.1:c.1652G>C	ENSP00000496741.1:n.1652G>C
ENST00000647015.1:c.1671+1254G>C	ENSP00000495389.1:n.1671+1254G>C
ENST00000647086.1:c.1678G>C	ENSP00000493677.1:p.Gly560Arg
ENST00000647158.1:c.1668+1254G>C	ENSP00000495744.1:n.1668+1254G>C
ENST00000302539.8:c.1681G>C	ENSP00000303960.4:p.Gly561Arg
ENST00000389817.7:c.1681G>C	ENSP00000374467.3:p.Gly561Arg
ENST00000526002.1:n.470G>C
ENST00000527905.5:c.1681G>C	ENSP00000431653.1:p.Gly561Arg
ENST00000528202.5:n.196G>C
ENST00000532728.5:n.1712G>C
NM_000352.4:c.1681G>C	NP_000343.2:p.Gly561Arg
NM_001287174.1:c.1681G>C	NP_001274103.1:p.Gly561Arg
XM_011520331.1:c.1678G>C	XP_011518633.1:p.Gly560Arg
XM_011520332.1:c.1681G>C	XP_011518634.1:p.Gly561Arg
XM_011520333.1:c.178G>C	XP_011518635.1:p.Gly60Arg
XM_011520334.1:c.1681G>C	XP_011518636.1:p.Gly561Arg
XR_930890.1:n.1744G>C
XR_930891.1:n.1744G>C
XR_930892.1:n.1744G>C
XR_930893.1:n.1744G>C
NM_001351295.1:c.1681G>C	NP_001338224.1:p.Gly561Arg
NM_001351296.1:c.1678G>C	NP_001338225.1:p.Gly560Arg
NM_001351297.1:c.1678G>C	NP_001338226.1:p.Gly560Arg
NR_147094.1:n.1747G>C
XM_017018197.2:c.1681G>C	XP_016873686.1:p.Gly561Arg
XM_017018199.1:c.1678G>C	XP_016873688.1:p.Gly560Arg
XM_017018201.2:c.1681G>C	XP_016873690.1:p.Gly561Arg
XM_017018202.1:c.178G>C	XP_016873691.1:p.Gly60Arg
XM_017018204.1:c.-363G>C	XP_016873693.1:n.-363G>C
XM_024448668.1:c.46G>C	XP_024304436.1:p.Gly16Arg
XR_001747945.2:n.1753G>C
XR_001747946.2:n.1753G>C
XR_002957189.1:n.1753G>C
NM_000352.6:c.1681G>C MANE Select	NP_000343.2:p.Gly561Arg
NM_001287174.2:c.1681G>C	NP_001274103.1:p.Gly561Arg
NM_001351295.2:c.1681G>C	NP_001338224.1:p.Gly561Arg
NM_001351296.2:c.1678G>C	NP_001338225.1:p.Gly560Arg
NM_001351297.2:c.1678G>C	NP_001338226.1:p.Gly560Arg
NR_147094.2:n.1747G>C
NM_001287174.3:c.1681G>C	NP_001274103.1:p.Gly561Arg