Canonical Allele Identifier: CA662761610

Gene: NEBL

Linked Data

• dbSNP Id: rs1185287321
• gnomAD v3: 10-20896847-CTG-C
• gnomAD v4: 10-20896847-CTG-C
• MyVariant Identifiers: chr10:g.21185777_21185778del (hg19) ; chr10:g.20896848_20896849del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.20896851_20896852del , CM000672.2:g.20896851_20896852del	GRCh38
NC_000010.10:g.21185780_21185781del , CM000672.1:g.21185780_21185781del	GRCh37
NC_000010.9:g.21225786_21225787del	NCBI36
NG_017092.1:g.282339_282340del , LRG_411:g.282339_282340del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377122.9:c.153+109_153+110del MANE Select	ENSP00000366326.4:n.153+109_153+110del
ENST00000674540.1:n.440+109_440+110del
ENST00000675114.1:n.565+64823_565+64824del
ENST00000675700.1:n.380+64823_380+64824del
ENST00000675702.1:n.636+64823_636+64824del
ENST00000675747.1:n.2515+109_2515+110del
ENST00000377119.5:n.163+109_163+110del
ENST00000377122.8:c.153+109_153+110del	ENSP00000366326.4:n.153+109_153+110del
ENST00000417816.2:c.357+64823_357+64824del	ENSP00000393896.2:n.357+64823_357+64824del
ENST00000434381.1:c.105+109_105+110del	ENSP00000396512.1:n.105+109_105+110del
NM_001173484.1:c.357+64823_357+64824del	NP_001166955.1:n.357+64823_357+64824del
NM_006393.2:c.153+109_153+110del , LRG_411t2:c.153+109_153+110del	NP_006384.1:n.153+109_153+110del
NM_213569.2:c.357+64823_357+64824del , LRG_411t1:c.357+64823_357+64824del	NP_998734.1:n.357+64823_357+64824del
XM_005252342.3:c.153+109_153+110del	XP_005252399.1:n.153+109_153+110del
XM_005252343.3:c.153+109_153+110del	XP_005252400.1:n.153+109_153+110del
XM_005252344.3:c.153+109_153+110del	XP_005252401.1:n.153+109_153+110del
XM_011519290.1:c.105+109_105+110del	XP_011517592.1:n.105+109_105+110del
XM_011519291.1:c.105+109_105+110del	XP_011517593.1:n.105+109_105+110del
XR_242691.3:n.265+109_265+110del
XM_005252342.5:c.153+109_153+110del	XP_005252399.1:n.153+109_153+110del
XM_005252343.5:c.153+109_153+110del	XP_005252400.1:n.153+109_153+110del
XM_005252344.5:c.153+109_153+110del	XP_005252401.1:n.153+109_153+110del
XM_011519291.2:c.105+109_105+110del	XP_011517593.1:n.105+109_105+110del
XM_017015468.1:c.105+109_105+110del	XP_016870957.1:n.105+109_105+110del
XR_001746995.2:n.1749+109_1749+110del
XR_001746996.1:n.468+109_468+110del
XR_242691.5:n.1749+109_1749+110del
NM_001173484.2:c.357+64823_357+64824del	NP_001166955.1:n.357+64823_357+64824del
NM_001377322.1:c.357+64823_357+64824del	NP_001364251.1:n.357+64823_357+64824del
NM_001377323.1:c.309+64823_309+64824del	NP_001364252.1:n.309+64823_309+64824del
NM_001377324.1:c.300+64823_300+64824del	NP_001364253.1:n.300+64823_300+64824del
NM_001377325.1:c.291+64823_291+64824del	NP_001364254.1:n.291+64823_291+64824del
NM_001377326.1:c.249+64823_249+64824del	NP_001364255.1:n.249+64823_249+64824del
NM_001377327.1:c.249+64823_249+64824del	NP_001364256.1:n.249+64823_249+64824del
NM_001377328.1:c.249+64823_249+64824del	NP_001364257.1:n.249+64823_249+64824del
NM_006393.3:c.153+109_153+110del MANE Select	NP_006384.1:n.153+109_153+110del