Canonical Allele Identifier: CA1895424061

Gene: NEBL

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.20896771_20896772delinsCA , CM000672.2:g.20896771_20896772delinsCA	GRCh38
NC_000010.10:g.21185700_21185701delinsCA , CM000672.1:g.21185700_21185701delinsCA	GRCh37
NC_000010.9:g.21225706_21225707delinsCA	NCBI36
NG_017092.1:g.282416_282417delinsTG , LRG_411:g.282416_282417delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377122.9:c.153+186_153+187delinsTG MANE Select	ENSP00000366326.4:n.153+186_153+187delinsTG
ENST00000674540.1:n.440+186_440+187delinsTG
ENST00000675114.1:n.565+64900_565+64901delinsTG
ENST00000675700.1:n.380+64900_380+64901delinsTG
ENST00000675702.1:n.636+64900_636+64901delinsTG
ENST00000675747.1:n.2515+186_2515+187delinsTG
ENST00000377119.5:n.163+186_163+187delinsTG
ENST00000377122.8:c.153+186_153+187delinsTG	ENSP00000366326.4:n.153+186_153+187delinsTG
ENST00000417816.2:c.357+64900_357+64901delinsTG	ENSP00000393896.2:n.357+64900_357+64901delinsTG
ENST00000434381.1:c.105+186_105+187delinsTG	ENSP00000396512.1:n.105+186_105+187delinsTG
NM_001173484.1:c.357+64900_357+64901delinsTG	NP_001166955.1:n.357+64900_357+64901delinsTG
NM_006393.2:c.153+186_153+187delinsTG , LRG_411t2:c.153+186_153+187delinsTG	NP_006384.1:n.153+186_153+187delinsTG
NM_213569.2:c.357+64900_357+64901delinsTG , LRG_411t1:c.357+64900_357+64901delinsTG	NP_998734.1:n.357+64900_357+64901delinsTG
XM_005252342.3:c.153+186_153+187delinsTG	XP_005252399.1:n.153+186_153+187delinsTG
XM_005252343.3:c.153+186_153+187delinsTG	XP_005252400.1:n.153+186_153+187delinsTG
XM_005252344.3:c.153+186_153+187delinsTG	XP_005252401.1:n.153+186_153+187delinsTG
XM_011519290.1:c.105+186_105+187delinsTG	XP_011517592.1:n.105+186_105+187delinsTG
XM_011519291.1:c.105+186_105+187delinsTG	XP_011517593.1:n.105+186_105+187delinsTG
XR_242691.3:n.265+186_265+187delinsTG
XM_005252342.5:c.153+186_153+187delinsTG	XP_005252399.1:n.153+186_153+187delinsTG
XM_005252343.5:c.153+186_153+187delinsTG	XP_005252400.1:n.153+186_153+187delinsTG
XM_005252344.5:c.153+186_153+187delinsTG	XP_005252401.1:n.153+186_153+187delinsTG
XM_011519291.2:c.105+186_105+187delinsTG	XP_011517593.1:n.105+186_105+187delinsTG
XM_017015468.1:c.105+186_105+187delinsTG	XP_016870957.1:n.105+186_105+187delinsTG
XR_001746995.2:n.1749+186_1749+187delinsTG
XR_001746996.1:n.468+186_468+187delinsTG
XR_242691.5:n.1749+186_1749+187delinsTG
NM_001173484.2:c.357+64900_357+64901delinsTG	NP_001166955.1:n.357+64900_357+64901delinsTG
NM_001377322.1:c.357+64900_357+64901delinsTG	NP_001364251.1:n.357+64900_357+64901delinsTG
NM_001377323.1:c.309+64900_309+64901delinsTG	NP_001364252.1:n.309+64900_309+64901delinsTG
NM_001377324.1:c.300+64900_300+64901delinsTG	NP_001364253.1:n.300+64900_300+64901delinsTG
NM_001377325.1:c.291+64900_291+64901delinsTG	NP_001364254.1:n.291+64900_291+64901delinsTG
NM_001377326.1:c.249+64900_249+64901delinsTG	NP_001364255.1:n.249+64900_249+64901delinsTG
NM_001377327.1:c.249+64900_249+64901delinsTG	NP_001364256.1:n.249+64900_249+64901delinsTG
NM_001377328.1:c.249+64900_249+64901delinsTG	NP_001364257.1:n.249+64900_249+64901delinsTG
NM_006393.3:c.153+186_153+187delinsTG MANE Select	NP_006384.1:n.153+186_153+187delinsTG