Canonical Allele Identifier: CA379791133

Gene: ABCC8

Linked Data

• MyVariant Identifiers: chr11:g.17418573T>A (hg19) ; chr11:g.17397026T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17397026T>A , CM000673.2:g.17397026T>A	GRCh38
NC_000011.9:g.17418573T>A , CM000673.1:g.17418573T>A	GRCh37
NC_000011.8:g.17375149T>A	NCBI36
NG_008867.1:g.84877A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524561.2:n.3610A>T
ENST00000528374.2:c.600A>T
ENST00000529967.6:n.2348A>T
ENST00000532220.2:n.2257A>T
ENST00000642611.2:n.4224A>T
ENST00000644057.2:n.452A>T
ENST00000645004.2:n.1508A>T
ENST00000682051.1:n.4171A>T
ENST00000682110.1:n.4224A>T
ENST00000682140.1:c.3985+167A>T	ENSP00000507829.1:n.3985+167A>T
ENST00000682185.1:n.5314A>T
ENST00000682204.1:c.*2147A>T	ENSP00000507094.1:n.*2147A>T
ENST00000682215.1:n.4591A>T
ENST00000682288.1:c.*2440A>T	ENSP00000507506.1:n.*2440A>T
ENST00000682442.1:n.4444A>T
ENST00000682528.1:n.4301A>T
ENST00000682673.1:n.4168A>T
ENST00000682805.1:n.4591A>T
ENST00000682965.1:c.*431A>T	ENSP00000508229.1:n.*431A>T
ENST00000683093.1:n.4323A>T
ENST00000683136.1:c.3892A>T	ENSP00000507768.1:p.Asn1298Tyr
ENST00000683153.1:n.4266A>T
ENST00000683365.1:n.4326A>T
ENST00000683377.1:n.4224A>T
ENST00000683456.1:c.*1146A>T	ENSP00000508318.1:n.*1146A>T
ENST00000683522.1:n.4224A>T
ENST00000683562.1:c.*2178A>T	ENSP00000508265.1:n.*2178A>T
ENST00000683693.1:n.4671A>T
ENST00000683725.1:c.4009A>T	ENSP00000507496.1:p.Asn1337Tyr
ENST00000684010.1:n.4219A>T
ENST00000684157.1:n.4224A>T
ENST00000684253.1:n.4127A>T
ENST00000684288.1:c.*2181A>T	ENSP00000507143.1:n.*2181A>T
ENST00000684313.1:n.3656A>T
ENST00000684332.1:n.4297A>T
ENST00000684371.1:n.4330A>T
ENST00000684404.1:n.4267A>T
ENST00000684442.1:n.4448A>T
ENST00000684555.1:c.*2221A>T	ENSP00000507705.1:n.*2221A>T
ENST00000684571.1:c.3850A>T	ENSP00000506935.1:p.Asn1284Tyr
ENST00000684593.1:c.*3714A>T	ENSP00000507005.1:n.*3714A>T
ENST00000684711.1:c.*2405A>T	ENSP00000506841.1:n.*2405A>T
ENST00000302539.9:c.4012A>T	ENSP00000303960.4:p.Asn1338Tyr
ENST00000389817.8:c.4009A>T MANE Select	ENSP00000374467.4:p.Asn1337Tyr
ENST00000642271.1:c.4006A>T	ENSP00000493749.1:p.Asn1336Tyr
ENST00000642579.1:c.2073-10A>T
ENST00000642611.1:n.4109A>T
ENST00000642902.1:c.3791A>T
ENST00000643260.1:c.4009A>T	ENSP00000494450.1:p.Asn1337Tyr
ENST00000643562.1:c.*2131A>T	ENSP00000496124.1:n.*2131A>T
ENST00000643925.1:c.2649A>T
ENST00000644057.1:n.86A>T
ENST00000644484.1:c.*2410A>T	ENSP00000493558.1:n.*2410A>T
ENST00000644675.1:c.*2181A>T	ENSP00000494567.1:n.*2181A>T
ENST00000644757.1:c.*2440A>T	ENSP00000495085.1:n.*2440A>T
ENST00000644772.1:c.4075A>T	ENSP00000494321.1:p.Asn1359Tyr
ENST00000645004.1:n.1664A>T
ENST00000645076.1:c.3208A>T
ENST00000645417.1:c.1197A>T
ENST00000645744.1:c.*2789A>T	ENSP00000494564.1:n.*2789A>T
ENST00000645760.1:c.4430A>T
ENST00000645884.1:c.*1292A>T	ENSP00000495516.1:n.*1292A>T
ENST00000646003.1:c.*2111A>T	ENSP00000495259.1:n.*2111A>T
ENST00000646207.1:c.*2846A>T	ENSP00000495025.1:n.*2846A>T
ENST00000646276.1:c.*2428A>T	ENSP00000496070.1:n.*2428A>T
ENST00000646592.1:c.3315A>T
ENST00000646902.1:c.3986-10A>T	ENSP00000494101.1:n.3986-10A>T
ENST00000646993.1:c.*2551A>T	ENSP00000493720.1:n.*2551A>T
ENST00000647013.1:c.4015A>T	ENSP00000496741.1:n.4015A>T
ENST00000647015.1:c.3760A>T	ENSP00000495389.1:p.Asn1254Tyr
ENST00000647086.1:c.*3605-10A>T	ENSP00000493677.1:n.*3605-10A>T
ENST00000647158.1:c.*2296A>T	ENSP00000495744.1:n.*2296A>T
ENST00000302539.8:c.4012A>T	ENSP00000303960.4:p.Asn1338Tyr
ENST00000389817.7:c.4009A>T	ENSP00000374467.3:p.Asn1337Tyr
ENST00000527905.5:c.*1031A>T	ENSP00000431653.1:n.*1031A>T
ENST00000528374.1:c.491A>T
ENST00000531137.1:n.574A>T
ENST00000531891.1:c.357-10A>T
ENST00000532220.1:n.483A>T
NM_000352.4:c.4009A>T	NP_000343.2:p.Asn1337Tyr
NM_001287174.1:c.4012A>T	NP_001274103.1:p.Asn1338Tyr
XM_011520331.1:c.4009A>T	XP_011518633.1:p.Asn1337Tyr
XM_011520332.1:c.4012A>T	XP_011518634.1:p.Asn1338Tyr
XM_011520333.1:c.2509A>T	XP_011518635.1:p.Asn837Tyr
XR_930890.1:n.4075A>T
NM_001351295.1:c.4075A>T	NP_001338224.1:p.Asn1359Tyr
NM_001351296.1:c.4009A>T	NP_001338225.1:p.Asn1337Tyr
NM_001351297.1:c.4006A>T	NP_001338226.1:p.Asn1336Tyr
NR_147094.1:n.4304A>T
XM_017018197.2:c.4078A>T	XP_016873686.1:p.Asn1360Tyr
XM_017018199.1:c.4075A>T	XP_016873688.1:p.Asn1359Tyr
XM_017018201.2:c.4078A>T	XP_016873690.1:p.Asn1360Tyr
XM_017018202.1:c.2575A>T	XP_016873691.1:p.Asn859Tyr
XM_017018204.1:c.1966A>T	XP_016873693.1:p.Asn656Tyr
XM_024448668.1:c.2377A>T	XP_024304436.1:p.Asn793Tyr
XR_001747945.2:n.4150A>T
XR_001747946.2:n.4081A>T
XR_002957189.1:n.4746A>T
NM_000352.6:c.4009A>T MANE Select	NP_000343.2:p.Asn1337Tyr
NM_001287174.2:c.4012A>T	NP_001274103.1:p.Asn1338Tyr
NM_001351295.2:c.4075A>T	NP_001338224.1:p.Asn1359Tyr
NM_001351296.2:c.4009A>T	NP_001338225.1:p.Asn1337Tyr
NM_001351297.2:c.4006A>T	NP_001338226.1:p.Asn1336Tyr
NR_147094.2:n.4304A>T
NM_001287174.3:c.4012A>T	NP_001274103.1:p.Asn1338Tyr