Canonical Allele Identifier: CA379781799

Gene: ABCC8

Linked Data

• MyVariant Identifiers: chr11:g.17415252T>A (hg19) ; chr11:g.17393705T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17393705T>A , CM000673.2:g.17393705T>A	GRCh38
NC_000011.9:g.17415252T>A , CM000673.1:g.17415252T>A	GRCh37
NC_000011.8:g.17371828T>A	NCBI36
NG_008867.1:g.88198A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524561.2:n.4201A>T
ENST00000526037.6:n.535A>T
ENST00000528374.2:c.1191A>T
ENST00000529967.6:n.2939A>T
ENST00000532220.2:n.3833A>T
ENST00000642611.2:n.5933A>T
ENST00000644057.2:n.1176A>T
ENST00000645004.2:n.2099A>T
ENST00000682051.1:n.4762A>T
ENST00000682110.1:n.4815A>T
ENST00000682140.1:c.*386A>T	ENSP00000507829.1:n.*386A>T
ENST00000682185.1:n.5905A>T
ENST00000682204.1:c.*2738A>T	ENSP00000507094.1:n.*2738A>T
ENST00000682215.1:n.5182A>T
ENST00000682288.1:c.*3031A>T	ENSP00000507506.1:n.*3031A>T
ENST00000682442.1:n.5035A>T
ENST00000682528.1:n.4892A>T
ENST00000682673.1:n.4759A>T
ENST00000682805.1:n.5220A>T
ENST00000682965.1:c.*1022A>T	ENSP00000508229.1:n.*1022A>T
ENST00000683093.1:n.5795A>T
ENST00000683136.1:c.4483A>T	ENSP00000507768.1:p.Thr1495Ser
ENST00000683153.1:n.4857A>T
ENST00000683365.1:n.4917A>T
ENST00000683377.1:n.4711A>T
ENST00000683456.1:c.*1737A>T	ENSP00000508318.1:n.*1737A>T
ENST00000683522.1:n.4897A>T
ENST00000683562.1:c.*2665A>T	ENSP00000508265.1:n.*2665A>T
ENST00000683693.1:n.6276A>T
ENST00000683725.1:c.*65A>T	ENSP00000507496.1:n.*65A>T
ENST00000684010.1:n.4810A>T
ENST00000684014.1:n.787A>T
ENST00000684157.1:n.5800A>T
ENST00000684253.1:n.4718A>T
ENST00000684288.1:c.*2772A>T	ENSP00000507143.1:n.*2772A>T
ENST00000684313.1:n.4247A>T
ENST00000684332.1:n.4888A>T
ENST00000684371.1:n.4921A>T
ENST00000684404.1:n.5843A>T
ENST00000684442.1:n.5039A>T
ENST00000684555.1:c.*2812A>T	ENSP00000507705.1:n.*2812A>T
ENST00000684571.1:c.4441A>T	ENSP00000506935.1:p.Thr1481Ser
ENST00000684593.1:c.*4305A>T	ENSP00000507005.1:n.*4305A>T
ENST00000684711.1:c.*2996A>T	ENSP00000506841.1:n.*2996A>T
ENST00000302539.9:c.4603A>T	ENSP00000303960.4:p.Thr1535Ser
ENST00000389817.8:c.4600A>T MANE Select	ENSP00000374467.4:p.Thr1534Ser
ENST00000642271.1:c.4597A>T	ENSP00000493749.1:p.Thr1533Ser
ENST00000642579.1:c.2654A>T
ENST00000642611.1:n.5818A>T
ENST00000642902.1:c.4382A>T
ENST00000643260.1:c.4600A>T	ENSP00000494450.1:p.Thr1534Ser
ENST00000643562.1:c.*2722A>T	ENSP00000496124.1:n.*2722A>T
ENST00000643925.1:c.3185+561A>T
ENST00000644057.1:n.759A>T
ENST00000644484.1:c.*3986A>T	ENSP00000493558.1:n.*3986A>T
ENST00000644675.1:c.*2772A>T	ENSP00000494567.1:n.*2772A>T
ENST00000644757.1:c.*3203-725A>T	ENSP00000495085.1:n.*3203-725A>T
ENST00000644772.1:c.4666A>T	ENSP00000494321.1:p.Thr1556Ser
ENST00000645004.1:n.2293A>T
ENST00000645076.1:c.3695A>T
ENST00000645417.1:c.1788A>T
ENST00000645744.1:c.*4285A>T	ENSP00000494564.1:n.*4285A>T
ENST00000645760.1:c.5021A>T
ENST00000645884.1:c.*1883A>T	ENSP00000495516.1:n.*1883A>T
ENST00000646003.1:c.*2622A>T	ENSP00000495259.1:n.*2622A>T
ENST00000646207.1:c.*3437A>T	ENSP00000495025.1:n.*3437A>T
ENST00000646276.1:c.*4004A>T	ENSP00000496070.1:n.*4004A>T
ENST00000646592.1:c.3906A>T
ENST00000646902.1:c.4567A>T	ENSP00000494101.1:p.Thr1523Ser
ENST00000646993.1:c.*3038A>T	ENSP00000493720.1:n.*3038A>T
ENST00000647015.1:c.4351A>T	ENSP00000495389.1:p.Thr1451Ser
ENST00000647086.1:c.*4186A>T	ENSP00000493677.1:n.*4186A>T
ENST00000647158.1:c.*2887A>T	ENSP00000495744.1:n.*2887A>T
ENST00000302539.8:c.4603A>T	ENSP00000303960.4:p.Thr1535Ser
ENST00000389817.7:c.4600A>T	ENSP00000374467.3:p.Thr1534Ser
ENST00000525022.1:n.495A>T
ENST00000526037.5:n.360A>T
ENST00000526168.5:c.388A>T
ENST00000531642.5:c.631A>T
NM_000352.4:c.4600A>T	NP_000343.2:p.Thr1534Ser
NM_001287174.1:c.4603A>T	NP_001274103.1:p.Thr1535Ser
XM_011520331.1:c.4600A>T	XP_011518633.1:p.Thr1534Ser
XM_011520333.1:c.3100A>T	XP_011518635.1:p.Thr1034Ser
XR_930890.1:n.4562A>T
NM_001351295.1:c.4666A>T	NP_001338224.1:p.Thr1556Ser
NM_001351296.1:c.4600A>T	NP_001338225.1:p.Thr1534Ser
NM_001351297.1:c.4597A>T	NP_001338226.1:p.Thr1533Ser
NR_147094.1:n.4895A>T
XM_017018197.2:c.4669A>T	XP_016873686.1:p.Thr1557Ser
XM_017018199.1:c.4666A>T	XP_016873688.1:p.Thr1556Ser
XM_017018202.1:c.3166A>T	XP_016873691.1:p.Thr1056Ser
XM_017018204.1:c.2557A>T	XP_016873693.1:p.Thr853Ser
XM_024448668.1:c.2968A>T	XP_024304436.1:p.Thr990Ser
XR_001747945.2:n.4637A>T
XR_001747946.2:n.4568A>T
XR_002957189.1:n.6351A>T
NM_000352.6:c.4600A>T MANE Select	NP_000343.2:p.Thr1534Ser
NM_001287174.2:c.4603A>T	NP_001274103.1:p.Thr1535Ser
NM_001351295.2:c.4666A>T	NP_001338224.1:p.Thr1556Ser
NM_001351296.2:c.4600A>T	NP_001338225.1:p.Thr1534Ser
NM_001351297.2:c.4597A>T	NP_001338226.1:p.Thr1533Ser
NR_147094.2:n.4895A>T
NM_001287174.3:c.4603A>T	NP_001274103.1:p.Thr1535Ser