Canonical Allele Identifier: CA597664823

Gene: ABCC8

Linked Data

• dbSNP Id: rs1172510830
• gnomAD v2: 11-17416696-G-A
• gnomAD v4: 11-17395149-G-A
• MyVariant Identifiers: chr11:g.17416696G>A (hg19) ; chr11:g.17395149G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17395149G>A , CM000673.2:g.17395149G>A	GRCh38
NC_000011.9:g.17416696G>A , CM000673.1:g.17416696G>A	GRCh37
NC_000011.8:g.17373272G>A	NCBI36
NG_008867.1:g.86754C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524561.2:n.4012+23C>T
ENST00000526037.6:n.346+23C>T
ENST00000528374.2:c.1002+23C>T
ENST00000529967.6:n.2750+23C>T
ENST00000532220.2:n.3644+23C>T
ENST00000642611.2:n.5744+23C>T
ENST00000644057.2:n.987+23C>T
ENST00000645004.2:n.1910+23C>T
ENST00000682051.1:n.4573+23C>T
ENST00000682110.1:n.4626+23C>T
ENST00000682140.1:c.*197+23C>T	ENSP00000507829.1:n.*197+23C>T
ENST00000682185.1:n.5716+23C>T
ENST00000682204.1:c.*2549+23C>T	ENSP00000507094.1:n.*2549+23C>T
ENST00000682215.1:n.4993+23C>T
ENST00000682288.1:c.*2842+23C>T	ENSP00000507506.1:n.*2842+23C>T
ENST00000682442.1:n.4846+23C>T
ENST00000682528.1:n.4703+23C>T
ENST00000682673.1:n.4570+23C>T
ENST00000682805.1:n.5031+23C>T
ENST00000682965.1:c.*833+23C>T	ENSP00000508229.1:n.*833+23C>T
ENST00000683093.1:n.5606+461C>T
ENST00000683136.1:c.4294+23C>T	ENSP00000507768.1:n.4294+23C>T
ENST00000683153.1:n.4668+23C>T
ENST00000683365.1:n.4728+23C>T
ENST00000683377.1:n.4522+461C>T
ENST00000683456.1:c.*1548+23C>T	ENSP00000508318.1:n.*1548+23C>T
ENST00000683522.1:n.4649C>T
ENST00000683562.1:c.*2476+461C>T	ENSP00000508265.1:n.*2476+461C>T
ENST00000683693.1:n.6087+461C>T
ENST00000683725.1:c.4307+461C>T	ENSP00000507496.1:n.4307+461C>T
ENST00000684010.1:n.4621+23C>T
ENST00000684157.1:n.5611+23C>T
ENST00000684253.1:n.4529+23C>T
ENST00000684288.1:c.*2583+23C>T	ENSP00000507143.1:n.*2583+23C>T
ENST00000684313.1:n.4058+23C>T
ENST00000684332.1:n.4699+23C>T
ENST00000684371.1:n.4732+23C>T
ENST00000684404.1:n.5654+23C>T
ENST00000684442.1:n.4850+23C>T
ENST00000684555.1:c.*2623+23C>T	ENSP00000507705.1:n.*2623+23C>T
ENST00000684571.1:c.4252+23C>T	ENSP00000506935.1:n.4252+23C>T
ENST00000684593.1:c.*4116+23C>T	ENSP00000507005.1:n.*4116+23C>T
ENST00000684711.1:c.*2807+23C>T	ENSP00000506841.1:n.*2807+23C>T
ENST00000302539.9:c.4414+23C>T	ENSP00000303960.4:n.4414+23C>T
ENST00000389817.8:c.4411+23C>T MANE Select	ENSP00000374467.4:n.4411+23C>T
ENST00000642271.1:c.4408+23C>T	ENSP00000493749.1:n.4408+23C>T
ENST00000642579.1:c.2465+23C>T
ENST00000642611.1:n.5629+23C>T
ENST00000642902.1:c.4193+23C>T
ENST00000643260.1:c.4411+23C>T	ENSP00000494450.1:n.4411+23C>T
ENST00000643562.1:c.*2533+23C>T	ENSP00000496124.1:n.*2533+23C>T
ENST00000643925.1:c.3051+23C>T
ENST00000644057.1:n.511C>T
ENST00000644484.1:c.*3797+23C>T	ENSP00000493558.1:n.*3797+23C>T
ENST00000644675.1:c.*2583+23C>T	ENSP00000494567.1:n.*2583+23C>T
ENST00000644757.1:c.*3202+1115C>T	ENSP00000495085.1:n.*3202+1115C>T
ENST00000644772.1:c.4477+23C>T	ENSP00000494321.1:n.4477+23C>T
ENST00000645004.1:n.2104+23C>T
ENST00000645076.1:c.3506+461C>T
ENST00000645417.1:c.1599+23C>T
ENST00000645744.1:c.*4096+23C>T	ENSP00000494564.1:n.*4096+23C>T
ENST00000645760.1:c.4832+23C>T
ENST00000645884.1:c.*1694+23C>T	ENSP00000495516.1:n.*1694+23C>T
ENST00000646003.1:c.*2433+23C>T	ENSP00000495259.1:n.*2433+23C>T
ENST00000646207.1:c.*3248+23C>T	ENSP00000495025.1:n.*3248+23C>T
ENST00000646276.1:c.*3815+23C>T	ENSP00000496070.1:n.*3815+23C>T
ENST00000646592.1:c.3717+23C>T
ENST00000646902.1:c.4378+23C>T	ENSP00000494101.1:n.4378+23C>T
ENST00000646993.1:c.*2849+461C>T	ENSP00000493720.1:n.*2849+461C>T
ENST00000647013.1:c.4417+23C>T	ENSP00000496741.1:n.4417+23C>T
ENST00000647015.1:c.4162+23C>T	ENSP00000495389.1:n.4162+23C>T
ENST00000647086.1:c.*3997+23C>T	ENSP00000493677.1:n.*3997+23C>T
ENST00000647158.1:c.*2698+23C>T	ENSP00000495744.1:n.*2698+23C>T
ENST00000302539.8:c.4414+23C>T	ENSP00000303960.4:n.4414+23C>T
ENST00000389817.7:c.4411+23C>T	ENSP00000374467.3:n.4411+23C>T
ENST00000525022.1:n.306+461C>T
ENST00000526037.5:n.171+461C>T
ENST00000526168.5:c.199+23C>T
ENST00000531642.5:c.442+23C>T
NM_000352.4:c.4411+23C>T	NP_000343.2:n.4411+23C>T
NM_001287174.1:c.4414+23C>T	NP_001274103.1:n.4414+23C>T
XM_011520331.1:c.4411+23C>T	XP_011518633.1:n.4411+23C>T
XM_011520332.1:c.4310+461C>T	XP_011518634.1:n.4310+461C>T
XM_011520333.1:c.2911+23C>T	XP_011518635.1:n.2911+23C>T
XR_930890.1:n.4373+461C>T
NM_001351295.1:c.4477+23C>T	NP_001338224.1:n.4477+23C>T
NM_001351296.1:c.4411+23C>T	NP_001338225.1:n.4411+23C>T
NM_001351297.1:c.4408+23C>T	NP_001338226.1:n.4408+23C>T
NR_147094.1:n.4706+23C>T
XM_017018197.2:c.4480+23C>T	XP_016873686.1:n.4480+23C>T
XM_017018199.1:c.4477+23C>T	XP_016873688.1:n.4477+23C>T
XM_017018201.2:c.4376+461C>T	XP_016873690.1:n.4376+461C>T
XM_017018202.1:c.2977+23C>T	XP_016873691.1:n.2977+23C>T
XM_017018204.1:c.2368+23C>T	XP_016873693.1:n.2368+23C>T
XM_024448668.1:c.2779+23C>T	XP_024304436.1:n.2779+23C>T
XR_001747945.2:n.4448+461C>T
XR_001747946.2:n.4379+461C>T
XR_002957189.1:n.6162+461C>T
NM_000352.6:c.4411+23C>T MANE Select	NP_000343.2:n.4411+23C>T
NM_001287174.2:c.4414+23C>T	NP_001274103.1:n.4414+23C>T
NM_001351295.2:c.4477+23C>T	NP_001338224.1:n.4477+23C>T
NM_001351296.2:c.4411+23C>T	NP_001338225.1:n.4411+23C>T
NM_001351297.2:c.4408+23C>T	NP_001338226.1:n.4408+23C>T
NR_147094.2:n.4706+23C>T
NM_001287174.3:c.4414+23C>T	NP_001274103.1:n.4414+23C>T