Canonical Allele Identifier: CA5902612

Gene: ABCC8

Linked Data

• dbSNP Id: rs764617363
• ExAC: 11:17418645 G / A
• gnomAD v2: 11-17418645-G-A
• gnomAD v3: 11-17397098-G-A
• gnomAD v4: 11-17397098-G-A
• MyVariant Identifiers: chr11:g.17418645G>A (hg19) ; chr11:g.17397098G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17397098G>A , CM000673.2:g.17397098G>A	GRCh38
NC_000011.9:g.17418645G>A , CM000673.1:g.17418645G>A	GRCh37
NC_000011.8:g.17375221G>A	NCBI36
NG_008867.1:g.84805C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524561.2:n.3538C>T
ENST00000528374.2:c.568-40C>T
ENST00000529967.6:n.2328-52C>T
ENST00000532220.2:n.2185C>T
ENST00000642611.2:n.4152C>T
ENST00000644057.2:n.432-52C>T
ENST00000645004.2:n.1488-52C>T
ENST00000682051.1:n.4099C>T
ENST00000682110.1:n.4152C>T
ENST00000682140.1:c.3985+95C>T	ENSP00000507829.1:n.3985+95C>T
ENST00000682185.1:n.5294-52C>T
ENST00000682204.1:c.*2127-52C>T	ENSP00000507094.1:n.*2127-52C>T
ENST00000682215.1:n.4519C>T
ENST00000682288.1:c.*2420-52C>T	ENSP00000507506.1:n.*2420-52C>T
ENST00000682442.1:n.4372C>T
ENST00000682528.1:n.4229C>T
ENST00000682673.1:n.4096C>T
ENST00000682805.1:n.4519C>T
ENST00000682965.1:c.*411-52C>T	ENSP00000508229.1:n.*411-52C>T
ENST00000683093.1:n.4251C>T
ENST00000683136.1:c.3872-52C>T	ENSP00000507768.1:n.3872-52C>T
ENST00000683153.1:n.4194C>T
ENST00000683365.1:n.4254C>T
ENST00000683377.1:n.4152C>T
ENST00000683456.1:c.*1126-52C>T	ENSP00000508318.1:n.*1126-52C>T
ENST00000683522.1:n.4152C>T
ENST00000683562.1:c.*2158-52C>T	ENSP00000508265.1:n.*2158-52C>T
ENST00000683693.1:n.4599C>T
ENST00000683725.1:c.3989-52C>T	ENSP00000507496.1:n.3989-52C>T
ENST00000684010.1:n.4147C>T
ENST00000684157.1:n.4152C>T
ENST00000684253.1:n.4055C>T
ENST00000684288.1:c.*2161-52C>T	ENSP00000507143.1:n.*2161-52C>T
ENST00000684313.1:n.3584C>T
ENST00000684332.1:n.4225C>T
ENST00000684371.1:n.4258C>T
ENST00000684404.1:n.4195C>T
ENST00000684442.1:n.4428-52C>T
ENST00000684555.1:c.*2201-52C>T	ENSP00000507705.1:n.*2201-52C>T
ENST00000684571.1:c.3830-52C>T	ENSP00000506935.1:n.3830-52C>T
ENST00000684593.1:c.*3694-52C>T	ENSP00000507005.1:n.*3694-52C>T
ENST00000684711.1:c.*2385-52C>T	ENSP00000506841.1:n.*2385-52C>T
ENST00000302539.9:c.3992-52C>T	ENSP00000303960.4:n.3992-52C>T
ENST00000389817.8:c.3989-52C>T MANE Select	ENSP00000374467.4:n.3989-52C>T
ENST00000642271.1:c.3986-52C>T	ENSP00000493749.1:n.3986-52C>T
ENST00000642579.1:c.2073-82C>T
ENST00000642611.1:n.4037C>T
ENST00000642902.1:c.3771-52C>T
ENST00000643260.1:c.3989-52C>T	ENSP00000494450.1:n.3989-52C>T
ENST00000643562.1:c.*2059C>T	ENSP00000496124.1:n.*2059C>T
ENST00000643925.1:c.2577C>T
ENST00000644057.1:n.14C>T
ENST00000644484.1:c.*2338C>T	ENSP00000493558.1:n.*2338C>T
ENST00000644675.1:c.*2161-52C>T	ENSP00000494567.1:n.*2161-52C>T
ENST00000644757.1:c.*2368C>T	ENSP00000495085.1:n.*2368C>T
ENST00000644772.1:c.4055-52C>T	ENSP00000494321.1:n.4055-52C>T
ENST00000645004.1:n.1592C>T
ENST00000645076.1:c.3188-52C>T
ENST00000645417.1:c.1177-52C>T
ENST00000645744.1:c.*2717C>T	ENSP00000494564.1:n.*2717C>T
ENST00000645760.1:c.4358C>T
ENST00000645884.1:c.*1220C>T	ENSP00000495516.1:n.*1220C>T
ENST00000646003.1:c.*2039C>T	ENSP00000495259.1:n.*2039C>T
ENST00000646207.1:c.*2826-52C>T	ENSP00000495025.1:n.*2826-52C>T
ENST00000646276.1:c.*2356C>T	ENSP00000496070.1:n.*2356C>T
ENST00000646592.1:c.3295-52C>T
ENST00000646902.1:c.3986-82C>T	ENSP00000494101.1:n.3986-82C>T
ENST00000646993.1:c.*2479C>T	ENSP00000493720.1:n.*2479C>T
ENST00000647013.1:c.3995-52C>T	ENSP00000496741.1:n.3995-52C>T
ENST00000647015.1:c.3740-52C>T	ENSP00000495389.1:n.3740-52C>T
ENST00000647086.1:c.*3605-82C>T	ENSP00000493677.1:n.*3605-82C>T
ENST00000647158.1:c.*2224C>T	ENSP00000495744.1:n.*2224C>T
ENST00000302539.8:c.3992-52C>T	ENSP00000303960.4:n.3992-52C>T
ENST00000389817.7:c.3989-52C>T	ENSP00000374467.3:n.3989-52C>T
ENST00000527905.5:c.*959C>T	ENSP00000431653.1:n.*959C>T
ENST00000528374.1:c.459-40C>T
ENST00000531137.1:n.502C>T
ENST00000531891.1:c.357-82C>T
ENST00000532220.1:n.411C>T
NM_000352.4:c.3989-52C>T	NP_000343.2:n.3989-52C>T
NM_001287174.1:c.3992-52C>T	NP_001274103.1:n.3992-52C>T
XM_011520331.1:c.3989-52C>T	XP_011518633.1:n.3989-52C>T
XM_011520332.1:c.3992-52C>T	XP_011518634.1:n.3992-52C>T
XM_011520333.1:c.2489-52C>T	XP_011518635.1:n.2489-52C>T
XR_930890.1:n.4055-52C>T
NM_001351295.1:c.4055-52C>T	NP_001338224.1:n.4055-52C>T
NM_001351296.1:c.3989-52C>T	NP_001338225.1:n.3989-52C>T
NM_001351297.1:c.3986-52C>T	NP_001338226.1:n.3986-52C>T
NR_147094.1:n.4232C>T
XM_017018197.2:c.4058-52C>T	XP_016873686.1:n.4058-52C>T
XM_017018199.1:c.4055-52C>T	XP_016873688.1:n.4055-52C>T
XM_017018201.2:c.4058-52C>T	XP_016873690.1:n.4058-52C>T
XM_017018202.1:c.2555-52C>T	XP_016873691.1:n.2555-52C>T
XM_017018204.1:c.1946-52C>T	XP_016873693.1:n.1946-52C>T
XM_024448668.1:c.2357-52C>T	XP_024304436.1:n.2357-52C>T
XR_001747945.2:n.4130-52C>T
XR_001747946.2:n.4061-52C>T
XR_002957189.1:n.4674C>T
NM_000352.6:c.3989-52C>T MANE Select	NP_000343.2:n.3989-52C>T
NM_001287174.2:c.3992-52C>T	NP_001274103.1:n.3992-52C>T
NM_001351295.2:c.4055-52C>T	NP_001338224.1:n.4055-52C>T
NM_001351296.2:c.3989-52C>T	NP_001338225.1:n.3989-52C>T
NM_001351297.2:c.3986-52C>T	NP_001338226.1:n.3986-52C>T
NR_147094.2:n.4232C>T
NM_001287174.3:c.3992-52C>T	NP_001274103.1:n.3992-52C>T