Canonical Allele Identifier: CA379816036

Gene: ABCC8

Linked Data

• MyVariant Identifiers: chr11:g.17450201C>A (hg19) ; chr11:g.17428654C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17428654C>A , CM000673.2:g.17428654C>A	GRCh38
NC_000011.9:g.17450201C>A , CM000673.1:g.17450201C>A	GRCh37
NC_000011.8:g.17406777C>A	NCBI36
NG_008867.1:g.53249G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524561.2:n.1503G>T
ENST00000642611.2:n.1900G>T
ENST00000682051.1:n.1847G>T
ENST00000682110.1:n.1900G>T
ENST00000682140.1:c.1831G>T	ENSP00000507829.1:p.Glu611Ter
ENST00000682185.1:n.3139G>T
ENST00000682204.1:c.1685G>T	ENSP00000507094.1:p.Arg562Leu
ENST00000682215.1:n.1900G>T
ENST00000682288.1:c.*262G>T	ENSP00000507506.1:n.*262G>T
ENST00000682442.1:n.2021G>T
ENST00000682528.1:n.1900G>T
ENST00000682673.1:n.1847G>T
ENST00000682805.1:n.1900G>T
ENST00000682965.1:c.1831G>T	ENSP00000508229.1:p.Glu611Ter
ENST00000683093.1:n.2002G>T
ENST00000683136.1:c.1831G>T	ENSP00000507768.1:p.Glu611Ter
ENST00000683153.1:n.1900G>T
ENST00000683253.1:n.2916G>T
ENST00000683365.1:n.2002G>T
ENST00000683377.1:n.1900G>T
ENST00000683456.1:c.1831G>T	ENSP00000508318.1:p.Glu611Ter
ENST00000683522.1:n.1900G>T
ENST00000683562.1:c.*3G>T	ENSP00000508265.1:n.*3G>T
ENST00000683693.1:n.1900G>T
ENST00000683725.1:c.1834G>T	ENSP00000507496.1:p.Glu612Ter
ENST00000684010.1:n.1900G>T
ENST00000684157.1:n.1900G>T
ENST00000684253.1:n.1806G>T
ENST00000684288.1:c.*3G>T	ENSP00000507143.1:n.*3G>T
ENST00000684313.1:n.1724-11692G>T
ENST00000684332.1:n.1973G>T
ENST00000684371.1:n.1847G>T
ENST00000684404.1:n.1900G>T
ENST00000684442.1:n.1900G>T
ENST00000684555.1:c.*43G>T	ENSP00000507705.1:n.*43G>T
ENST00000684571.1:c.1675G>T	ENSP00000506935.1:p.Glu559Ter
ENST00000684593.1:c.*1539G>T	ENSP00000507005.1:n.*1539G>T
ENST00000684711.1:c.*230G>T	ENSP00000506841.1:n.*230G>T
ENST00000302539.9:c.1834G>T	ENSP00000303960.4:p.Glu612Ter
ENST00000389817.8:c.1834G>T MANE Select	ENSP00000374467.4:p.Glu612Ter
ENST00000532728.6:c.1415G>T
ENST00000642271.1:c.1831G>T	ENSP00000493749.1:p.Glu611Ter
ENST00000642611.1:n.1785G>T
ENST00000642902.1:c.1669G>T
ENST00000643260.1:c.1831G>T	ENSP00000494450.1:p.Glu611Ter
ENST00000643562.1:c.1834G>T	ENSP00000496124.1:p.Glu612Ter
ENST00000644447.1:c.187G>T	ENSP00000496282.1:p.Glu63Ter
ENST00000644472.1:c.*195G>T	ENSP00000495378.1:n.*195G>T
ENST00000644484.1:c.*43G>T	ENSP00000493558.1:n.*43G>T
ENST00000644542.1:c.*1536G>T	ENSP00000495532.1:n.*1536G>T
ENST00000644649.1:c.1004G>T
ENST00000644675.1:c.*3G>T	ENSP00000494567.1:n.*3G>T
ENST00000644757.1:c.*136G>T	ENSP00000495085.1:n.*136G>T
ENST00000644772.1:c.1834G>T	ENSP00000494321.1:p.Glu612Ter
ENST00000645076.1:c.1100-14G>T
ENST00000645744.1:c.*195G>T	ENSP00000494564.1:n.*195G>T
ENST00000645760.1:c.2109G>T
ENST00000645884.1:c.1831G>T	ENSP00000495516.1:p.Glu611Ter
ENST00000646003.1:c.1685G>T	ENSP00000495259.1:p.Arg562Leu
ENST00000646207.1:c.*195G>T	ENSP00000495025.1:n.*195G>T
ENST00000646276.1:c.*104G>T	ENSP00000496070.1:n.*104G>T
ENST00000646592.1:c.898G>T
ENST00000646902.1:c.1831G>T	ENSP00000494101.1:p.Glu611Ter
ENST00000646993.1:c.*230G>T	ENSP00000493720.1:n.*230G>T
ENST00000647013.1:c.1837G>T	ENSP00000496741.1:n.1837G>T
ENST00000647015.1:c.1672-249G>T	ENSP00000495389.1:n.1672-249G>T
ENST00000647086.1:c.*1561G>T	ENSP00000493677.1:n.*1561G>T
ENST00000647158.1:c.1685G>T	ENSP00000495744.1:p.Arg562Leu
ENST00000302539.8:c.1834G>T	ENSP00000303960.4:p.Glu612Ter
ENST00000389817.7:c.1834G>T	ENSP00000374467.3:p.Glu612Ter
ENST00000527905.5:c.1818-14G>T	ENSP00000431653.1:n.1818-14G>T
NM_000352.4:c.1834G>T	NP_000343.2:p.Glu612Ter
NM_001287174.1:c.1834G>T	NP_001274103.1:p.Glu612Ter
XM_011520331.1:c.1831G>T	XP_011518633.1:p.Glu611Ter
XM_011520332.1:c.1834G>T	XP_011518634.1:p.Glu612Ter
XM_011520333.1:c.331G>T	XP_011518635.1:p.Glu111Ter
XM_011520334.1:c.1834G>T	XP_011518636.1:p.Glu612Ter
XR_930890.1:n.1897G>T
XR_930891.1:n.1897G>T
XR_930892.1:n.1897G>T
XR_930893.1:n.1897G>T
NM_001351295.1:c.1834G>T	NP_001338224.1:p.Glu612Ter
NM_001351296.1:c.1831G>T	NP_001338225.1:p.Glu611Ter
NM_001351297.1:c.1831G>T	NP_001338226.1:p.Glu611Ter
NR_147094.1:n.1900G>T
XM_017018197.2:c.1834G>T	XP_016873686.1:p.Glu612Ter
XM_017018199.1:c.1831G>T	XP_016873688.1:p.Glu611Ter
XM_017018201.2:c.1834G>T	XP_016873690.1:p.Glu612Ter
XM_017018202.1:c.331G>T	XP_016873691.1:p.Glu111Ter
XM_017018204.1:c.-210G>T	XP_016873693.1:n.-210G>T
XM_024448668.1:c.199G>T	XP_024304436.1:p.Glu67Ter
XR_001747945.2:n.1906G>T
XR_001747946.2:n.1906G>T
XR_002957189.1:n.1906G>T
NM_000352.6:c.1834G>T MANE Select	NP_000343.2:p.Glu612Ter
NM_001287174.2:c.1834G>T	NP_001274103.1:p.Glu612Ter
NM_001351295.2:c.1834G>T	NP_001338224.1:p.Glu612Ter
NM_001351296.2:c.1831G>T	NP_001338225.1:p.Glu611Ter
NM_001351297.2:c.1831G>T	NP_001338226.1:p.Glu611Ter
NR_147094.2:n.1900G>T
NM_001287174.3:c.1834G>T	NP_001274103.1:p.Glu612Ter