Canonical Allele Identifier: CA5903710

Gene: ABCC8

Linked Data

• ClinVar Variation Id: 2146773
• ClinVar RCV Id: RCV003076848
• dbSNP Id: rs751181213
• ExAC: 11:17482062 C / A
• gnomAD v2: 11-17482062-C-A
• gnomAD v3: 11-17460515-C-A
• gnomAD v4: 11-17460515-C-A
• MyVariant Identifiers: chr11:g.17482062C>A (hg19) ; chr11:g.17460515C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17460515C>A , CM000673.2:g.17460515C>A	GRCh38
NC_000011.9:g.17482062C>A , CM000673.1:g.17482062C>A	GRCh37
NC_000011.8:g.17438638C>A	NCBI36
NG_008867.1:g.21388G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000524561.2:n.648+2923G>T
ENST00000526002.2:n.997G>T
ENST00000528202.6:n.1050G>T
ENST00000642611.2:n.1050G>T
ENST00000682051.1:n.997G>T
ENST00000682091.1:n.1959G>T
ENST00000682110.1:n.1050G>T
ENST00000682140.1:c.981G>T	ENSP00000507829.1:p.Gly327=
ENST00000682199.1:n.1050G>T
ENST00000682204.1:c.981G>T	ENSP00000507094.1:p.Gly327=
ENST00000682215.1:n.1050G>T
ENST00000682288.1:c.981G>T	ENSP00000507506.1:p.Gly327=
ENST00000682442.1:n.1084G>T
ENST00000682528.1:n.1050G>T
ENST00000682673.1:n.997G>T
ENST00000682805.1:n.1050G>T
ENST00000682863.1:n.1050G>T
ENST00000682965.1:c.981G>T	ENSP00000508229.1:p.Gly327=
ENST00000683093.1:n.1050G>T
ENST00000683136.1:c.981G>T	ENSP00000507768.1:p.Gly327=
ENST00000683153.1:n.1050G>T
ENST00000683253.1:n.1964G>T
ENST00000683365.1:n.1050G>T
ENST00000683377.1:n.1050G>T
ENST00000683456.1:c.981G>T	ENSP00000508318.1:p.Gly327=
ENST00000683522.1:n.1050G>T
ENST00000683531.1:n.1053G>T
ENST00000683562.1:c.984G>T	ENSP00000508265.1:p.Gly328=
ENST00000683693.1:n.1050G>T
ENST00000683725.1:c.984G>T	ENSP00000507496.1:p.Gly328=
ENST00000683808.1:n.320G>T
ENST00000684010.1:n.1050G>T
ENST00000684157.1:n.1050G>T
ENST00000684221.1:n.1820G>T
ENST00000684253.1:n.1102G>T
ENST00000684288.1:c.984G>T	ENSP00000507143.1:p.Gly328=
ENST00000684313.1:n.1077G>T
ENST00000684332.1:n.1050G>T
ENST00000684371.1:n.997G>T
ENST00000684404.1:n.1050G>T
ENST00000684442.1:n.1050G>T
ENST00000684555.1:c.984G>T	ENSP00000507705.1:p.Gly328=
ENST00000684571.1:c.981G>T	ENSP00000506935.1:p.Gly327=
ENST00000684593.1:c.*689G>T	ENSP00000507005.1:n.*689G>T
ENST00000684711.1:c.981G>T	ENSP00000506841.1:p.Gly327=
ENST00000302539.9:c.984G>T	ENSP00000303960.4:p.Gly328=
ENST00000389817.8:c.984G>T MANE Select	ENSP00000374467.4:p.Gly328=
ENST00000532728.6:c.860G>T
ENST00000635881.1:n.1012G>T
ENST00000642271.1:c.981G>T	ENSP00000493749.1:p.Gly327=
ENST00000642611.1:n.935G>T
ENST00000642902.1:c.965G>T
ENST00000643260.1:c.981G>T	ENSP00000494450.1:p.Gly327=
ENST00000643562.1:c.984G>T	ENSP00000496124.1:p.Gly328=
ENST00000644472.1:c.981G>T	ENSP00000495378.1:p.Gly327=
ENST00000644484.1:c.981G>T	ENSP00000493558.1:p.Gly327=
ENST00000644542.1:c.*686G>T	ENSP00000495532.1:n.*686G>T
ENST00000644649.1:c.34G>T
ENST00000644675.1:c.981G>T	ENSP00000494567.1:p.Gly327=
ENST00000644757.1:c.984G>T	ENSP00000495085.1:p.Gly328=
ENST00000644772.1:c.984G>T	ENSP00000494321.1:p.Gly328=
ENST00000645076.1:c.266G>T
ENST00000645744.1:c.981G>T	ENSP00000494564.1:p.Gly327=
ENST00000645760.1:c.1157G>T
ENST00000645884.1:c.981G>T	ENSP00000495516.1:p.Gly327=
ENST00000646003.1:c.981G>T	ENSP00000495259.1:p.Gly327=
ENST00000646207.1:c.981G>T	ENSP00000495025.1:p.Gly327=
ENST00000646276.1:c.960G>T	ENSP00000496070.1:p.Gly320=
ENST00000646592.1:c.235G>T
ENST00000646737.1:c.*1078G>T	ENSP00000494874.1:n.*1078G>T
ENST00000646902.1:c.981G>T	ENSP00000494101.1:p.Gly327=
ENST00000646993.1:c.984G>T	ENSP00000493720.1:p.Gly328=
ENST00000647013.1:c.882G>T	ENSP00000496741.1:p.Gly294=
ENST00000647015.1:c.984G>T	ENSP00000495389.1:p.Gly328=
ENST00000647086.1:c.981G>T	ENSP00000493677.1:p.Gly327=
ENST00000647158.1:c.981G>T	ENSP00000495744.1:p.Gly327=
ENST00000302539.8:c.984G>T	ENSP00000303960.4:p.Gly328=
ENST00000389817.7:c.984G>T	ENSP00000374467.3:p.Gly328=
ENST00000527905.5:c.984G>T	ENSP00000431653.1:p.Gly328=
ENST00000532728.5:n.1015G>T
NM_000352.4:c.984G>T	NP_000343.2:p.Gly328=
NM_001287174.1:c.984G>T	NP_001274103.1:p.Gly328=
XM_011520331.1:c.981G>T	XP_011518633.1:p.Gly327=
XM_011520332.1:c.984G>T	XP_011518634.1:p.Gly328=
XM_011520334.1:c.984G>T	XP_011518636.1:p.Gly328=
XR_930890.1:n.1047G>T
XR_930891.1:n.1047G>T
XR_930892.1:n.1047G>T
XR_930893.1:n.1047G>T
NM_001351295.1:c.984G>T	NP_001338224.1:p.Gly328=
NM_001351296.1:c.981G>T	NP_001338225.1:p.Gly327=
NM_001351297.1:c.981G>T	NP_001338226.1:p.Gly327=
NR_147094.1:n.1050G>T
XM_017018197.2:c.984G>T	XP_016873686.1:p.Gly328=
XM_017018199.1:c.981G>T	XP_016873688.1:p.Gly327=
XM_017018201.2:c.984G>T	XP_016873690.1:p.Gly328=
XM_017018202.1:c.-534G>T	XP_016873691.1:n.-534G>T
XM_024448668.1:c.-754G>T	XP_024304436.1:n.-754G>T
XR_001747945.2:n.1056G>T
XR_001747946.2:n.1056G>T
XR_002957189.1:n.1056G>T
NM_000352.6:c.984G>T MANE Select	NP_000343.2:p.Gly328=
NM_001287174.2:c.984G>T	NP_001274103.1:p.Gly328=
NM_001351295.2:c.984G>T	NP_001338224.1:p.Gly328=
NM_001351296.2:c.981G>T	NP_001338225.1:p.Gly327=
NM_001351297.2:c.981G>T	NP_001338226.1:p.Gly327=
NR_147094.2:n.1050G>T
NM_001287174.3:c.984G>T	NP_001274103.1:p.Gly328=