Canonical Allele Identifier: CA1895424080
Gene: NEBL HGNC NCBI

Linked Data

dbSNP Id: rs1847535981

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.20896804_20896805insTTCAGGTCTTTGAAATTTCAGT , CM000672.2:g.20896804_20896805insTTCAGGTCTTTGAAATTTCAGT GRCh38
NC_000010.10:g.21185733_21185734insTTCAGGTCTTTGAAATTTCAGT , CM000672.1:g.21185733_21185734insTTCAGGTCTTTGAAATTTCAGT GRCh37
NC_000010.9:g.21225739_21225740insTTCAGGTCTTTGAAATTTCAGT NCBI36
NG_017092.1:g.282384_282385insCTGAAATTTCAAAGACCTGAAA , LRG_411:g.282384_282385insCTGAAATTTCAAAGACCTGAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000377122.9:c.153+154_153+155insCTGAAATTTCAAAGACCTGAAA MANE Select ENSP00000366326.4:n.153+154_153+155insCTGAAATTTCAAAGACCTGAAA
ENST00000674540.1:n.440+154_440+155insCTGAAATTTCAAAGACCTGAAA
ENST00000675114.1:n.565+64868_565+64869insCTGAAATTTCAAAGACCTGAAA
ENST00000675700.1:n.380+64868_380+64869insCTGAAATTTCAAAGACCTGAAA
ENST00000675702.1:n.636+64868_636+64869insCTGAAATTTCAAAGACCTGAAA
ENST00000675747.1:n.2515+154_2515+155insCTGAAATTTCAAAGACCTGAAA
ENST00000377119.5:n.163+154_163+155insCTGAAATTTCAAAGACCTGAAA
ENST00000377122.8:c.153+154_153+155insCTGAAATTTCAAAGACCTGAAA ENSP00000366326.4:n.153+154_153+155insCTGAAATTTCAAAGACCTGAAA
ENST00000417816.2:c.357+64868_357+64869insCTGAAATTTCAAAGACCTGAAA ENSP00000393896.2:n.357+64868_357+64869insCTGAAATTTCAAAGACCTG...
ENST00000434381.1:c.105+154_105+155insCTGAAATTTCAAAGACCTGAAA ENSP00000396512.1:n.105+154_105+155insCTGAAATTTCAAAGACCTGAAA
NM_001173484.1:c.357+64868_357+64869insCTGAAATTTCAAAGACCTGAAA NP_001166955.1:n.357+64868_357+64869insCTGAAATTTCAAAGACCTGAAA...
NM_006393.2:c.153+154_153+155insCTGAAATTTCAAAGACCTGAAA , LRG_411t2:c.153+154_153+155insCTGAAATTTCAAAGACCTGAAA NP_006384.1:n.153+154_153+155insCTGAAATTTCAAAGACCTGAAA
NM_213569.2:c.357+64868_357+64869insCTGAAATTTCAAAGACCTGAAA , LRG_411t1:c.357+64868_357+64869insCTGAAATTTCAAAGACCTGAAA NP_998734.1:n.357+64868_357+64869insCTGAAATTTCAAAGACCTGAAA
XM_005252342.3:c.153+154_153+155insCTGAAATTTCAAAGACCTGAAA XP_005252399.1:n.153+154_153+155insCTGAAATTTCAAAGACCTGAAA
XM_005252343.3:c.153+154_153+155insCTGAAATTTCAAAGACCTGAAA XP_005252400.1:n.153+154_153+155insCTGAAATTTCAAAGACCTGAAA
XM_005252344.3:c.153+154_153+155insCTGAAATTTCAAAGACCTGAAA XP_005252401.1:n.153+154_153+155insCTGAAATTTCAAAGACCTGAAA
XM_011519290.1:c.105+154_105+155insCTGAAATTTCAAAGACCTGAAA XP_011517592.1:n.105+154_105+155insCTGAAATTTCAAAGACCTGAAA
XM_011519291.1:c.105+154_105+155insCTGAAATTTCAAAGACCTGAAA XP_011517593.1:n.105+154_105+155insCTGAAATTTCAAAGACCTGAAA
XR_242691.3:n.265+154_265+155insCTGAAATTTCAAAGACCTGAAA
XM_005252342.5:c.153+154_153+155insCTGAAATTTCAAAGACCTGAAA XP_005252399.1:n.153+154_153+155insCTGAAATTTCAAAGACCTGAAA
XM_005252343.5:c.153+154_153+155insCTGAAATTTCAAAGACCTGAAA XP_005252400.1:n.153+154_153+155insCTGAAATTTCAAAGACCTGAAA
XM_005252344.5:c.153+154_153+155insCTGAAATTTCAAAGACCTGAAA XP_005252401.1:n.153+154_153+155insCTGAAATTTCAAAGACCTGAAA
XM_011519291.2:c.105+154_105+155insCTGAAATTTCAAAGACCTGAAA XP_011517593.1:n.105+154_105+155insCTGAAATTTCAAAGACCTGAAA
XM_017015468.1:c.105+154_105+155insCTGAAATTTCAAAGACCTGAAA XP_016870957.1:n.105+154_105+155insCTGAAATTTCAAAGACCTGAAA
XR_001746995.2:n.1749+154_1749+155insCTGAAATTTCAAAGACCTGAAA
XR_001746996.1:n.468+154_468+155insCTGAAATTTCAAAGACCTGAAA
XR_242691.5:n.1749+154_1749+155insCTGAAATTTCAAAGACCTGAAA
NM_001173484.2:c.357+64868_357+64869insCTGAAATTTCAAAGACCTGAAA NP_001166955.1:n.357+64868_357+64869insCTGAAATTTCAAAGACCTGAAA...
NM_001377322.1:c.357+64868_357+64869insCTGAAATTTCAAAGACCTGAAA NP_001364251.1:n.357+64868_357+64869insCTGAAATTTCAAAGACCTGAAA...
NM_001377323.1:c.309+64868_309+64869insCTGAAATTTCAAAGACCTGAAA NP_001364252.1:n.309+64868_309+64869insCTGAAATTTCAAAGACCTGAAA...
NM_001377324.1:c.300+64868_300+64869insCTGAAATTTCAAAGACCTGAAA NP_001364253.1:n.300+64868_300+64869insCTGAAATTTCAAAGACCTGAAA...
NM_001377325.1:c.291+64868_291+64869insCTGAAATTTCAAAGACCTGAAA NP_001364254.1:n.291+64868_291+64869insCTGAAATTTCAAAGACCTGAAA...
NM_001377326.1:c.249+64868_249+64869insCTGAAATTTCAAAGACCTGAAA NP_001364255.1:n.249+64868_249+64869insCTGAAATTTCAAAGACCTGAAA...
NM_001377327.1:c.249+64868_249+64869insCTGAAATTTCAAAGACCTGAAA NP_001364256.1:n.249+64868_249+64869insCTGAAATTTCAAAGACCTGAAA...
NM_001377328.1:c.249+64868_249+64869insCTGAAATTTCAAAGACCTGAAA NP_001364257.1:n.249+64868_249+64869insCTGAAATTTCAAAGACCTGAAA...
NM_006393.3:c.153+154_153+155insCTGAAATTTCAAAGACCTGAAA MANE Select NP_006384.1:n.153+154_153+155insCTGAAATTTCAAAGACCTGAAA