Canonical Allele Identifier: CA1895393938

Gene: NEBL

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.20897040_20897045delinsAAAAAG , CM000672.2:g.20897040_20897045delinsAAAAAG	GRCh38
NC_000010.10:g.21185969_21185974delinsAAAAAG , CM000672.1:g.21185969_21185974delinsAAAAAG	GRCh37
NC_000010.9:g.21225975_21225980delinsAAAAAG	NCBI36
NG_017092.1:g.282143_282148delinsCTTTTT , LRG_411:g.282143_282148delinsCTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377122.9:c.82-16_82-11delinsCTTTTT MANE Select	ENSP00000366326.4:n.82-16_82-11delinsCTTTTT
ENST00000674540.1:n.369-16_369-11delinsCTTTTT
ENST00000675114.1:n.565+64627_565+64632delinsCTTTTT
ENST00000675700.1:n.380+64627_380+64632delinsCTTTTT
ENST00000675702.1:n.636+64627_636+64632delinsCTTTTT
ENST00000675747.1:n.2444-16_2444-11delinsCTTTTT
ENST00000377119.5:n.92-16_92-11delinsCTTTTT
ENST00000377122.8:c.82-16_82-11delinsCTTTTT	ENSP00000366326.4:n.82-16_82-11delinsCTTTTT
ENST00000417816.2:c.357+64627_357+64632delinsCTTTTT	ENSP00000393896.2:n.357+64627_357+64632delinsCTTTTT
ENST00000434381.1:c.34-16_34-11delinsCTTTTT	ENSP00000396512.1:n.34-16_34-11delinsCTTTTT
NM_001173484.1:c.357+64627_357+64632delinsCTTTTT	NP_001166955.1:n.357+64627_357+64632delinsCTTTTT
NM_006393.2:c.82-16_82-11delinsCTTTTT , LRG_411t2:c.82-16_82-11delinsCTTTTT	NP_006384.1:n.82-16_82-11delinsCTTTTT
NM_213569.2:c.357+64627_357+64632delinsCTTTTT , LRG_411t1:c.357+64627_357+64632delinsCTTTTT	NP_998734.1:n.357+64627_357+64632delinsCTTTTT
XM_005252342.3:c.82-16_82-11delinsCTTTTT	XP_005252399.1:n.82-16_82-11delinsCTTTTT
XM_005252343.3:c.82-16_82-11delinsCTTTTT	XP_005252400.1:n.82-16_82-11delinsCTTTTT
XM_005252344.3:c.82-16_82-11delinsCTTTTT	XP_005252401.1:n.82-16_82-11delinsCTTTTT
XM_011519290.1:c.34-16_34-11delinsCTTTTT	XP_011517592.1:n.34-16_34-11delinsCTTTTT
XM_011519291.1:c.34-16_34-11delinsCTTTTT	XP_011517593.1:n.34-16_34-11delinsCTTTTT
XR_242691.3:n.194-16_194-11delinsCTTTTT
XM_005252342.5:c.82-16_82-11delinsCTTTTT	XP_005252399.1:n.82-16_82-11delinsCTTTTT
XM_005252343.5:c.82-16_82-11delinsCTTTTT	XP_005252400.1:n.82-16_82-11delinsCTTTTT
XM_005252344.5:c.82-16_82-11delinsCTTTTT	XP_005252401.1:n.82-16_82-11delinsCTTTTT
XM_011519291.2:c.34-16_34-11delinsCTTTTT	XP_011517593.1:n.34-16_34-11delinsCTTTTT
XM_017015468.1:c.34-16_34-11delinsCTTTTT	XP_016870957.1:n.34-16_34-11delinsCTTTTT
XR_001746995.2:n.1678-16_1678-11delinsCTTTTT
XR_001746996.1:n.397-16_397-11delinsCTTTTT
XR_242691.5:n.1678-16_1678-11delinsCTTTTT
NM_001173484.2:c.357+64627_357+64632delinsCTTTTT	NP_001166955.1:n.357+64627_357+64632delinsCTTTTT
NM_001377322.1:c.357+64627_357+64632delinsCTTTTT	NP_001364251.1:n.357+64627_357+64632delinsCTTTTT
NM_001377323.1:c.309+64627_309+64632delinsCTTTTT	NP_001364252.1:n.309+64627_309+64632delinsCTTTTT
NM_001377324.1:c.300+64627_300+64632delinsCTTTTT	NP_001364253.1:n.300+64627_300+64632delinsCTTTTT
NM_001377325.1:c.291+64627_291+64632delinsCTTTTT	NP_001364254.1:n.291+64627_291+64632delinsCTTTTT
NM_001377326.1:c.249+64627_249+64632delinsCTTTTT	NP_001364255.1:n.249+64627_249+64632delinsCTTTTT
NM_001377327.1:c.249+64627_249+64632delinsCTTTTT	NP_001364256.1:n.249+64627_249+64632delinsCTTTTT
NM_001377328.1:c.249+64627_249+64632delinsCTTTTT	NP_001364257.1:n.249+64627_249+64632delinsCTTTTT
NM_006393.3:c.82-16_82-11delinsCTTTTT MANE Select	NP_006384.1:n.82-16_82-11delinsCTTTTT