Canonical Allele Identifier: CA218406375

Gene: ABCC8

Linked Data

• dbSNP Id: rs1031534135
• gnomAD v2: 11-17415335-T-C
• MyVariant Identifiers: chr11:g.17415335T>C (hg19) ; chr11:g.17393788T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17393788T>C , CM000673.2:g.17393788T>C	GRCh38
NC_000011.9:g.17415335T>C , CM000673.1:g.17415335T>C	GRCh37
NC_000011.8:g.17371911T>C	NCBI36
NG_008867.1:g.88115A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000524561.2:n.4147-29A>G
ENST00000526037.6:n.481-29A>G
ENST00000528374.2:c.1137-29A>G
ENST00000529967.6:n.2885-29A>G
ENST00000532220.2:n.3779-29A>G
ENST00000642611.2:n.5879-29A>G
ENST00000644057.2:n.1122-29A>G
ENST00000645004.2:n.2045-29A>G
ENST00000682051.1:n.4708-29A>G
ENST00000682110.1:n.4761-29A>G
ENST00000682140.1:c.*332-29A>G	ENSP00000507829.1:n.*332-29A>G
ENST00000682185.1:n.5851-29A>G
ENST00000682204.1:c.*2684-29A>G	ENSP00000507094.1:n.*2684-29A>G
ENST00000682215.1:n.5128-29A>G
ENST00000682288.1:c.*2977-29A>G	ENSP00000507506.1:n.*2977-29A>G
ENST00000682442.1:n.4981-29A>G
ENST00000682528.1:n.4838-29A>G
ENST00000682673.1:n.4705-29A>G
ENST00000682805.1:n.5166-29A>G
ENST00000682965.1:c.*968-29A>G	ENSP00000508229.1:n.*968-29A>G
ENST00000683093.1:n.5741-29A>G
ENST00000683136.1:c.4429-29A>G	ENSP00000507768.1:n.4429-29A>G
ENST00000683153.1:n.4803-29A>G
ENST00000683365.1:n.4863-29A>G
ENST00000683377.1:n.4657-29A>G
ENST00000683456.1:c.*1683-29A>G	ENSP00000508318.1:n.*1683-29A>G
ENST00000683522.1:n.4843-29A>G
ENST00000683562.1:c.*2611-29A>G	ENSP00000508265.1:n.*2611-29A>G
ENST00000683693.1:n.6222-29A>G
ENST00000683725.1:c.*11-29A>G	ENSP00000507496.1:n.*11-29A>G
ENST00000684010.1:n.4756-29A>G
ENST00000684014.1:n.733-29A>G
ENST00000684157.1:n.5746-29A>G
ENST00000684253.1:n.4664-29A>G
ENST00000684288.1:c.*2718-29A>G	ENSP00000507143.1:n.*2718-29A>G
ENST00000684313.1:n.4193-29A>G
ENST00000684332.1:n.4834-29A>G
ENST00000684371.1:n.4867-29A>G
ENST00000684404.1:n.5789-29A>G
ENST00000684442.1:n.4985-29A>G
ENST00000684555.1:c.*2758-29A>G	ENSP00000507705.1:n.*2758-29A>G
ENST00000684571.1:c.4387-29A>G	ENSP00000506935.1:n.4387-29A>G
ENST00000684593.1:c.*4251-29A>G	ENSP00000507005.1:n.*4251-29A>G
ENST00000684711.1:c.*2942-29A>G	ENSP00000506841.1:n.*2942-29A>G
ENST00000302539.9:c.4549-29A>G	ENSP00000303960.4:n.4549-29A>G
ENST00000389817.8:c.4546-29A>G MANE Select	ENSP00000374467.4:n.4546-29A>G
ENST00000642271.1:c.4543-29A>G	ENSP00000493749.1:n.4543-29A>G
ENST00000642579.1:c.2600-29A>G
ENST00000642611.1:n.5764-29A>G
ENST00000642902.1:c.4328-29A>G
ENST00000643260.1:c.4546-29A>G	ENSP00000494450.1:n.4546-29A>G
ENST00000643562.1:c.*2668-29A>G	ENSP00000496124.1:n.*2668-29A>G
ENST00000643925.1:c.3185+478A>G
ENST00000644057.1:n.705-29A>G
ENST00000644484.1:c.*3932-29A>G	ENSP00000493558.1:n.*3932-29A>G
ENST00000644675.1:c.*2718-29A>G	ENSP00000494567.1:n.*2718-29A>G
ENST00000644757.1:c.*3203-808A>G	ENSP00000495085.1:n.*3203-808A>G
ENST00000644772.1:c.4612-29A>G	ENSP00000494321.1:n.4612-29A>G
ENST00000645004.1:n.2239-29A>G
ENST00000645076.1:c.3641-29A>G
ENST00000645417.1:c.1734-29A>G
ENST00000645744.1:c.*4231-29A>G	ENSP00000494564.1:n.*4231-29A>G
ENST00000645760.1:c.4967-29A>G
ENST00000645884.1:c.*1829-29A>G	ENSP00000495516.1:n.*1829-29A>G
ENST00000646003.1:c.*2568-29A>G	ENSP00000495259.1:n.*2568-29A>G
ENST00000646207.1:c.*3383-29A>G	ENSP00000495025.1:n.*3383-29A>G
ENST00000646276.1:c.*3950-29A>G	ENSP00000496070.1:n.*3950-29A>G
ENST00000646592.1:c.3852-29A>G
ENST00000646902.1:c.4513-29A>G	ENSP00000494101.1:n.4513-29A>G
ENST00000646993.1:c.*2984-29A>G	ENSP00000493720.1:n.*2984-29A>G
ENST00000647015.1:c.4297-29A>G	ENSP00000495389.1:n.4297-29A>G
ENST00000647086.1:c.*4132-29A>G	ENSP00000493677.1:n.*4132-29A>G
ENST00000647158.1:c.*2833-29A>G	ENSP00000495744.1:n.*2833-29A>G
ENST00000302539.8:c.4549-29A>G	ENSP00000303960.4:n.4549-29A>G
ENST00000389817.7:c.4546-29A>G	ENSP00000374467.3:n.4546-29A>G
ENST00000525022.1:n.441-29A>G
ENST00000526037.5:n.306-29A>G
ENST00000526168.5:c.334-29A>G
ENST00000531642.5:c.577-29A>G
NM_000352.4:c.4546-29A>G	NP_000343.2:n.4546-29A>G
NM_001287174.1:c.4549-29A>G	NP_001274103.1:n.4549-29A>G
XM_011520331.1:c.4546-29A>G	XP_011518633.1:n.4546-29A>G
XM_011520333.1:c.3046-29A>G	XP_011518635.1:n.3046-29A>G
XR_930890.1:n.4508-29A>G
NM_001351295.1:c.4612-29A>G	NP_001338224.1:n.4612-29A>G
NM_001351296.1:c.4546-29A>G	NP_001338225.1:n.4546-29A>G
NM_001351297.1:c.4543-29A>G	NP_001338226.1:n.4543-29A>G
NR_147094.1:n.4841-29A>G
XM_017018197.2:c.4615-29A>G	XP_016873686.1:n.4615-29A>G
XM_017018199.1:c.4612-29A>G	XP_016873688.1:n.4612-29A>G
XM_017018202.1:c.3112-29A>G	XP_016873691.1:n.3112-29A>G
XM_017018204.1:c.2503-29A>G	XP_016873693.1:n.2503-29A>G
XM_024448668.1:c.2914-29A>G	XP_024304436.1:n.2914-29A>G
XR_001747945.2:n.4583-29A>G
XR_001747946.2:n.4514-29A>G
XR_002957189.1:n.6297-29A>G
NM_000352.6:c.4546-29A>G MANE Select	NP_000343.2:n.4546-29A>G
NM_001287174.2:c.4549-29A>G	NP_001274103.1:n.4549-29A>G
NM_001351295.2:c.4612-29A>G	NP_001338224.1:n.4612-29A>G
NM_001351296.2:c.4546-29A>G	NP_001338225.1:n.4546-29A>G
NM_001351297.2:c.4543-29A>G	NP_001338226.1:n.4543-29A>G
NR_147094.2:n.4841-29A>G
NM_001287174.3:c.4549-29A>G	NP_001274103.1:n.4549-29A>G