Canonical Allele Identifier: CA1895393954
Gene: NEBL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.20897076T= , CM000672.2:g.20897076T= GRCh38
NC_000010.10:g.21186005T= , CM000672.1:g.21186005T= GRCh37
NC_000010.9:g.21226011T= NCBI36
NG_017092.1:g.282112A= , LRG_411:g.282112A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000377122.9:c.82-47A= MANE Select ENSP00000366326.4:n.82-47A=
ENST00000674540.1:n.369-47A=
ENST00000675114.1:n.565+64596A=
ENST00000675700.1:n.380+64596A=
ENST00000675702.1:n.636+64596A=
ENST00000675747.1:n.2444-47A=
ENST00000377119.5:n.92-47A=
ENST00000377122.8:c.82-47A= ENSP00000366326.4:n.82-47A=
ENST00000417816.2:c.357+64596A= ENSP00000393896.2:n.357+64596A=
ENST00000434381.1:c.34-47A= ENSP00000396512.1:n.34-47A=
NM_001173484.1:c.357+64596A= NP_001166955.1:n.357+64596A=
NM_006393.2:c.82-47A= , LRG_411t2:c.82-47A= NP_006384.1:n.82-47A=
NM_213569.2:c.357+64596A= , LRG_411t1:c.357+64596A= NP_998734.1:n.357+64596A=
XM_005252342.3:c.82-47A= XP_005252399.1:n.82-47A=
XM_005252343.3:c.82-47A= XP_005252400.1:n.82-47A=
XM_005252344.3:c.82-47A= XP_005252401.1:n.82-47A=
XM_011519290.1:c.34-47A= XP_011517592.1:n.34-47A=
XM_011519291.1:c.34-47A= XP_011517593.1:n.34-47A=
XR_242691.3:n.194-47A=
XM_005252342.5:c.82-47A= XP_005252399.1:n.82-47A=
XM_005252343.5:c.82-47A= XP_005252400.1:n.82-47A=
XM_005252344.5:c.82-47A= XP_005252401.1:n.82-47A=
XM_011519291.2:c.34-47A= XP_011517593.1:n.34-47A=
XM_017015468.1:c.34-47A= XP_016870957.1:n.34-47A=
XR_001746995.2:n.1678-47A=
XR_001746996.1:n.397-47A=
XR_242691.5:n.1678-47A=
NM_001173484.2:c.357+64596A= NP_001166955.1:n.357+64596A=
NM_001377322.1:c.357+64596A= NP_001364251.1:n.357+64596A=
NM_001377323.1:c.309+64596A= NP_001364252.1:n.309+64596A=
NM_001377324.1:c.300+64596A= NP_001364253.1:n.300+64596A=
NM_001377325.1:c.291+64596A= NP_001364254.1:n.291+64596A=
NM_001377326.1:c.249+64596A= NP_001364255.1:n.249+64596A=
NM_001377327.1:c.249+64596A= NP_001364256.1:n.249+64596A=
NM_001377328.1:c.249+64596A= NP_001364257.1:n.249+64596A=
NM_006393.3:c.82-47A= MANE Select NP_006384.1:n.82-47A=