Canonical Allele Identifier: CA376098734
Gene: NEBL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.20897016G>T , CM000672.2:g.20897016G>T GRCh38
NC_000010.10:g.21185945G>T , CM000672.1:g.21185945G>T GRCh37
NC_000010.9:g.21225951G>T NCBI36
NG_017092.1:g.282172C>A , LRG_411:g.282172C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000377122.9:c.95C>A MANE Select ENSP00000366326.4:p.Pro32His
ENST00000674540.1:n.382C>A
ENST00000675114.1:n.565+64656C>A
ENST00000675700.1:n.380+64656C>A
ENST00000675702.1:n.636+64656C>A
ENST00000675747.1:n.2457C>A
ENST00000377119.5:n.105C>A
ENST00000377122.8:c.95C>A ENSP00000366326.4:p.Pro32His
ENST00000417816.2:c.357+64656C>A ENSP00000393896.2:n.357+64656C>A
ENST00000434381.1:c.47C>A ENSP00000396512.1:p.Pro16His
NM_001173484.1:c.357+64656C>A NP_001166955.1:n.357+64656C>A
NM_006393.2:c.95C>A , LRG_411t2:c.95C>A NP_006384.1:p.Pro32His
NM_213569.2:c.357+64656C>A , LRG_411t1:c.357+64656C>A NP_998734.1:n.357+64656C>A
XM_005252342.3:c.95C>A XP_005252399.1:p.Pro32His
XM_005252343.3:c.95C>A XP_005252400.1:p.Pro32His
XM_005252344.3:c.95C>A XP_005252401.1:p.Pro32His
XM_011519290.1:c.47C>A XP_011517592.1:p.Pro16His
XM_011519291.1:c.47C>A XP_011517593.1:p.Pro16His
XR_242691.3:n.207C>A
XM_005252342.5:c.95C>A XP_005252399.1:p.Pro32His
XM_005252343.5:c.95C>A XP_005252400.1:p.Pro32His
XM_005252344.5:c.95C>A XP_005252401.1:p.Pro32His
XM_011519291.2:c.47C>A XP_011517593.1:p.Pro16His
XM_017015468.1:c.47C>A XP_016870957.1:p.Pro16His
XR_001746995.2:n.1691C>A
XR_001746996.1:n.410C>A
XR_242691.5:n.1691C>A
NM_001173484.2:c.357+64656C>A NP_001166955.1:n.357+64656C>A
NM_001377322.1:c.357+64656C>A NP_001364251.1:n.357+64656C>A
NM_001377323.1:c.309+64656C>A NP_001364252.1:n.309+64656C>A
NM_001377324.1:c.300+64656C>A NP_001364253.1:n.300+64656C>A
NM_001377325.1:c.291+64656C>A NP_001364254.1:n.291+64656C>A
NM_001377326.1:c.249+64656C>A NP_001364255.1:n.249+64656C>A
NM_001377327.1:c.249+64656C>A NP_001364256.1:n.249+64656C>A
NM_001377328.1:c.249+64656C>A NP_001364257.1:n.249+64656C>A
NM_006393.3:c.95C>A MANE Select NP_006384.1:p.Pro32His