Canonical Allele Identifier: CA2612664434

Gene: ABCC8

Linked Data

• gnomAD v4: 11-17428099-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17428099A>G , CM000673.2:g.17428099A>G	GRCh38
NC_000011.9:g.17449646A>G , CM000673.1:g.17449646A>G	GRCh37
NC_000011.8:g.17406222A>G	NCBI36
NG_008867.1:g.53804T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524561.2:n.1710-157T>C
ENST00000529967.6:n.300-157T>C
ENST00000642611.2:n.2107-157T>C
ENST00000682051.1:n.2054-157T>C
ENST00000682110.1:n.2107-157T>C
ENST00000682140.1:c.2038-157T>C	ENSP00000507829.1:n.2038-157T>C
ENST00000682185.1:n.3346-157T>C
ENST00000682204.1:c.*179-157T>C	ENSP00000507094.1:n.*179-157T>C
ENST00000682215.1:n.2107-157T>C
ENST00000682288.1:c.*469-157T>C	ENSP00000507506.1:n.*469-157T>C
ENST00000682442.1:n.2228-157T>C
ENST00000682528.1:n.2107-157T>C
ENST00000682673.1:n.2054-157T>C
ENST00000682805.1:n.2107-157T>C
ENST00000682965.1:c.2038-157T>C	ENSP00000508229.1:n.2038-157T>C
ENST00000683093.1:n.2209-157T>C
ENST00000683136.1:c.2038-157T>C	ENSP00000507768.1:n.2038-157T>C
ENST00000683153.1:n.2266-157T>C
ENST00000683253.1:n.3123-157T>C
ENST00000683365.1:n.2209-157T>C
ENST00000683377.1:n.2107-157T>C
ENST00000683456.1:c.2038-157T>C	ENSP00000508318.1:n.2038-157T>C
ENST00000683522.1:n.2107-157T>C
ENST00000683562.1:c.*210-157T>C	ENSP00000508265.1:n.*210-157T>C
ENST00000683693.1:n.2107-157T>C
ENST00000683725.1:c.2041-157T>C	ENSP00000507496.1:n.2041-157T>C
ENST00000684010.1:n.2107-157T>C
ENST00000684157.1:n.2107-157T>C
ENST00000684253.1:n.2013-157T>C
ENST00000684288.1:c.*210-157T>C	ENSP00000507143.1:n.*210-157T>C
ENST00000684313.1:n.1724-11137T>C
ENST00000684332.1:n.2180-157T>C
ENST00000684371.1:n.2213-157T>C
ENST00000684404.1:n.2107-157T>C
ENST00000684442.1:n.2107-157T>C
ENST00000684555.1:c.*250-157T>C	ENSP00000507705.1:n.*250-157T>C
ENST00000684571.1:c.1882-157T>C	ENSP00000506935.1:n.1882-157T>C
ENST00000684593.1:c.*1746-157T>C	ENSP00000507005.1:n.*1746-157T>C
ENST00000684711.1:c.*437-157T>C	ENSP00000506841.1:n.*437-157T>C
ENST00000302539.9:c.2041-157T>C	ENSP00000303960.4:n.2041-157T>C
ENST00000389817.8:c.2041-157T>C MANE Select	ENSP00000374467.4:n.2041-157T>C
ENST00000532728.6:c.1622-157T>C
ENST00000642271.1:c.2038-157T>C	ENSP00000493749.1:n.2038-157T>C
ENST00000642579.1:c.122-157T>C
ENST00000642611.1:n.1992-157T>C
ENST00000642902.1:c.1876-157T>C
ENST00000643260.1:c.2038-157T>C	ENSP00000494450.1:n.2038-157T>C
ENST00000643562.1:c.*17-157T>C	ENSP00000496124.1:n.*17-157T>C
ENST00000644447.1:c.394-157T>C	ENSP00000496282.1:n.394-157T>C
ENST00000644472.1:c.*402-157T>C	ENSP00000495378.1:n.*402-157T>C
ENST00000644484.1:c.*250-157T>C	ENSP00000493558.1:n.*250-157T>C
ENST00000644542.1:c.*1743-157T>C	ENSP00000495532.1:n.*1743-157T>C
ENST00000644649.1:c.1211-157T>C
ENST00000644675.1:c.*210-157T>C	ENSP00000494567.1:n.*210-157T>C
ENST00000644757.1:c.*343-157T>C	ENSP00000495085.1:n.*343-157T>C
ENST00000644772.1:c.2107-157T>C	ENSP00000494321.1:n.2107-157T>C
ENST00000645076.1:c.1293-157T>C
ENST00000645744.1:c.*402-157T>C	ENSP00000494564.1:n.*402-157T>C
ENST00000645760.1:c.2316-157T>C
ENST00000645884.1:c.2038-157T>C	ENSP00000495516.1:n.2038-157T>C
ENST00000646003.1:c.*179-157T>C	ENSP00000495259.1:n.*179-157T>C
ENST00000646207.1:c.*402-157T>C	ENSP00000495025.1:n.*402-157T>C
ENST00000646276.1:c.*311-157T>C	ENSP00000496070.1:n.*311-157T>C
ENST00000646592.1:c.1264-157T>C
ENST00000646902.1:c.2038-157T>C	ENSP00000494101.1:n.2038-157T>C
ENST00000646993.1:c.*437-157T>C	ENSP00000493720.1:n.*437-157T>C
ENST00000647013.1:c.2044-157T>C	ENSP00000496741.1:n.2044-157T>C
ENST00000647015.1:c.1789-157T>C	ENSP00000495389.1:n.1789-157T>C
ENST00000647086.1:c.*1768-157T>C	ENSP00000493677.1:n.*1768-157T>C
ENST00000647158.1:c.*179-157T>C	ENSP00000495744.1:n.*179-157T>C
ENST00000302539.8:c.2041-157T>C	ENSP00000303960.4:n.2041-157T>C
ENST00000389817.7:c.2041-157T>C	ENSP00000374467.3:n.2041-157T>C
ENST00000527905.5:c.2011-157T>C	ENSP00000431653.1:n.2011-157T>C
NM_000352.4:c.2041-157T>C	NP_000343.2:n.2041-157T>C
NM_001287174.1:c.2041-157T>C	NP_001274103.1:n.2041-157T>C
XM_011520331.1:c.2038-157T>C	XP_011518633.1:n.2038-157T>C
XM_011520332.1:c.2041-157T>C	XP_011518634.1:n.2041-157T>C
XM_011520333.1:c.538-157T>C	XP_011518635.1:n.538-157T>C
XM_011520334.1:c.2041-157T>C	XP_011518636.1:n.2041-157T>C
XR_930890.1:n.2104-157T>C
XR_930891.1:n.2104-157T>C
XR_930892.1:n.2104-157T>C
XR_930893.1:n.2104-157T>C
NM_001351295.1:c.2107-157T>C	NP_001338224.1:n.2107-157T>C
NM_001351296.1:c.2038-157T>C	NP_001338225.1:n.2038-157T>C
NM_001351297.1:c.2038-157T>C	NP_001338226.1:n.2038-157T>C
NR_147094.1:n.2107-157T>C
XM_017018197.2:c.2107-157T>C	XP_016873686.1:n.2107-157T>C
XM_017018199.1:c.2104-157T>C	XP_016873688.1:n.2104-157T>C
XM_017018201.2:c.2107-157T>C	XP_016873690.1:n.2107-157T>C
XM_017018202.1:c.604-157T>C	XP_016873691.1:n.604-157T>C
XM_017018204.1:c.-3-157T>C	XP_016873693.1:n.-3-157T>C
XM_024448668.1:c.406-157T>C	XP_024304436.1:n.406-157T>C
XR_001747945.2:n.2179-157T>C
XR_001747946.2:n.2113-157T>C
XR_002957189.1:n.2179-157T>C
NM_000352.6:c.2041-157T>C MANE Select	NP_000343.2:n.2041-157T>C
NM_001287174.2:c.2041-157T>C	NP_001274103.1:n.2041-157T>C
NM_001351295.2:c.2107-157T>C	NP_001338224.1:n.2107-157T>C
NM_001351296.2:c.2038-157T>C	NP_001338225.1:n.2038-157T>C
NM_001351297.2:c.2038-157T>C	NP_001338226.1:n.2038-157T>C
NR_147094.2:n.2107-157T>C
NM_001287174.3:c.2041-157T>C	NP_001274103.1:n.2041-157T>C