Canonical Allele Identifier: CA1895393940

Gene: NEBL

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.20897047_20897050delinsAAAG , CM000672.2:g.20897047_20897050delinsAAAG	GRCh38
NC_000010.10:g.21185976_21185979delinsAAAG , CM000672.1:g.21185976_21185979delinsAAAG	GRCh37
NC_000010.9:g.21225982_21225985delinsAAAG	NCBI36
NG_017092.1:g.282138_282141delinsCTTT , LRG_411:g.282138_282141delinsCTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377122.9:c.82-21_82-18delinsCTTT MANE Select	ENSP00000366326.4:n.82-21_82-18delinsCTTT
ENST00000674540.1:n.369-21_369-18delinsCTTT
ENST00000675114.1:n.565+64622_565+64625delinsCTTT
ENST00000675700.1:n.380+64622_380+64625delinsCTTT
ENST00000675702.1:n.636+64622_636+64625delinsCTTT
ENST00000675747.1:n.2444-21_2444-18delinsCTTT
ENST00000377119.5:n.92-21_92-18delinsCTTT
ENST00000377122.8:c.82-21_82-18delinsCTTT	ENSP00000366326.4:n.82-21_82-18delinsCTTT
ENST00000417816.2:c.357+64622_357+64625delinsCTTT	ENSP00000393896.2:n.357+64622_357+64625delinsCTTT
ENST00000434381.1:c.34-21_34-18delinsCTTT	ENSP00000396512.1:n.34-21_34-18delinsCTTT
NM_001173484.1:c.357+64622_357+64625delinsCTTT	NP_001166955.1:n.357+64622_357+64625delinsCTTT
NM_006393.2:c.82-21_82-18delinsCTTT , LRG_411t2:c.82-21_82-18delinsCTTT	NP_006384.1:n.82-21_82-18delinsCTTT
NM_213569.2:c.357+64622_357+64625delinsCTTT , LRG_411t1:c.357+64622_357+64625delinsCTTT	NP_998734.1:n.357+64622_357+64625delinsCTTT
XM_005252342.3:c.82-21_82-18delinsCTTT	XP_005252399.1:n.82-21_82-18delinsCTTT
XM_005252343.3:c.82-21_82-18delinsCTTT	XP_005252400.1:n.82-21_82-18delinsCTTT
XM_005252344.3:c.82-21_82-18delinsCTTT	XP_005252401.1:n.82-21_82-18delinsCTTT
XM_011519290.1:c.34-21_34-18delinsCTTT	XP_011517592.1:n.34-21_34-18delinsCTTT
XM_011519291.1:c.34-21_34-18delinsCTTT	XP_011517593.1:n.34-21_34-18delinsCTTT
XR_242691.3:n.194-21_194-18delinsCTTT
XM_005252342.5:c.82-21_82-18delinsCTTT	XP_005252399.1:n.82-21_82-18delinsCTTT
XM_005252343.5:c.82-21_82-18delinsCTTT	XP_005252400.1:n.82-21_82-18delinsCTTT
XM_005252344.5:c.82-21_82-18delinsCTTT	XP_005252401.1:n.82-21_82-18delinsCTTT
XM_011519291.2:c.34-21_34-18delinsCTTT	XP_011517593.1:n.34-21_34-18delinsCTTT
XM_017015468.1:c.34-21_34-18delinsCTTT	XP_016870957.1:n.34-21_34-18delinsCTTT
XR_001746995.2:n.1678-21_1678-18delinsCTTT
XR_001746996.1:n.397-21_397-18delinsCTTT
XR_242691.5:n.1678-21_1678-18delinsCTTT
NM_001173484.2:c.357+64622_357+64625delinsCTTT	NP_001166955.1:n.357+64622_357+64625delinsCTTT
NM_001377322.1:c.357+64622_357+64625delinsCTTT	NP_001364251.1:n.357+64622_357+64625delinsCTTT
NM_001377323.1:c.309+64622_309+64625delinsCTTT	NP_001364252.1:n.309+64622_309+64625delinsCTTT
NM_001377324.1:c.300+64622_300+64625delinsCTTT	NP_001364253.1:n.300+64622_300+64625delinsCTTT
NM_001377325.1:c.291+64622_291+64625delinsCTTT	NP_001364254.1:n.291+64622_291+64625delinsCTTT
NM_001377326.1:c.249+64622_249+64625delinsCTTT	NP_001364255.1:n.249+64622_249+64625delinsCTTT
NM_001377327.1:c.249+64622_249+64625delinsCTTT	NP_001364256.1:n.249+64622_249+64625delinsCTTT
NM_001377328.1:c.249+64622_249+64625delinsCTTT	NP_001364257.1:n.249+64622_249+64625delinsCTTT
NM_006393.3:c.82-21_82-18delinsCTTT MANE Select	NP_006384.1:n.82-21_82-18delinsCTTT