Canonical Allele Identifier: CA2220652502
Gene: ABCC11 HGNC NCBI

Linked Data

dbSNP Id: rs387906296

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.48167589_48167615dup , CM000678.2:g.48167589_48167615dup GRCh38
NC_000016.9:g.48201500_48201526dup , CM000678.1:g.48201500_48201526dup GRCh37
NC_000016.8:g.46759001_46759027dup NCBI36
NG_011522.1:g.72565_72591dup

Transcript Alleles

HGVS Amino-acid change
ENST00000356608.7:c.3939_3965dup MANE Select ENSP00000349017.2:p.Arg1321_Glu1322insAsp...
ENST00000353782.9:c.3825_3851dup ENSP00000311326.6:p.Arg1283_Glu1284insAsp...
ENST00000356608.6:c.3939_3965dup ENSP00000349017.2:p.Arg1321_Glu1322insAsp...
ENST00000394747.5:c.3939_3965dup ENSP00000378230.1:p.Arg1321_Glu1322insAsp...
ENST00000394748.5:c.3939_3965dup ENSP00000378231.1:p.Arg1321_Glu1322insAsp...
ENST00000565329.1:n.1239_1265dup
NM_032583.3:c.3939_3965dup NP_115972.2:p.Arg1321_Glu1322insAspThrLeu...
NM_033151.3:c.3939_3965dup NP_149163.2:p.Arg1321_Glu1322insAspThrLeu...
NM_145186.2:c.3825_3851dup NP_660187.1:p.Arg1283_Glu1284insAspThrLeu...
XM_011523396.1:c.3741_3767dup XP_011521698.1:p.Arg1255_Glu1256insAspThr...
XM_011523397.1:c.2982_3008dup XP_011521699.1:p.Arg1002_Glu1003insAspThr...
XM_011523398.1:c.2070_2096dup XP_011521700.1:p.Arg698_Glu699insAspThrLe...
XM_011523397.2:c.2982_3008dup XP_011521699.1:p.Arg1002_Glu1003insAspThr...
XM_011523398.3:c.2070_2096dup XP_011521700.1:p.Arg698_Glu699insAspThrLe...
XM_017023795.2:c.3939_3965dup XP_016879284.1:p.Arg1321_Glu1322insAspThr...
XM_017023796.2:c.3939_3965dup XP_016879285.1:p.Arg1321_Glu1322insAspThr...
XM_017023797.2:c.3939_3965dup XP_016879286.1:p.Arg1321_Glu1322insAspThr...
XM_017023798.2:c.3939_3965dup XP_016879287.1:p.Arg1321_Glu1322insAspThr...
XM_017023799.2:c.3939_3965dup XP_016879288.1:p.Arg1321_Glu1322insAspThr...
XM_017023800.2:c.3939_3965dup XP_016879289.1:p.Arg1321_Glu1322insAspThr...
XM_017023801.2:c.3831_3857dup XP_016879290.1:p.Arg1285_Glu1286insAspThr...
XM_017023802.2:c.2982_3008dup XP_016879291.1:p.Arg1002_Glu1003insAspThr...
XM_024450475.1:c.2982_3008dup XP_024306243.1:p.Arg1002_Glu1003insAspThr...
XR_001752012.1:n.6617_6643dup
NM_001370496.1:c.3945_3971dup NP_001357425.1:p.Arg1323_Glu1324insAspThr...
NM_001370497.1:c.3939_3965dup MANE Select NP_001357426.1:p.Arg1321_Glu1322insAspThr...
NM_032583.4:c.3939_3965dup NP_115972.2:p.Arg1321_Glu1322insAspThrLeu...
NM_033151.4:c.3939_3965dup NP_149163.2:p.Arg1321_Glu1322insAspThrLeu...
NM_145186.3:c.3825_3851dup NP_660187.1:p.Arg1283_Glu1284insAspThrLeu...