Canonical Allele Identifier: CA662761605

Gene: NEBL

Linked Data

• dbSNP Id: rs1478364496
• MyVariant Identifiers: chr10:g.21185751_21185752del (hg19) ; chr10:g.20896822_20896823del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.20896822_20896823del , CM000672.2:g.20896822_20896823del	GRCh38
NC_000010.10:g.21185751_21185752del , CM000672.1:g.21185751_21185752del	GRCh37
NC_000010.9:g.21225757_21225758del	NCBI36
NG_017092.1:g.282365_282366del , LRG_411:g.282365_282366del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377122.9:c.153+135_153+136del MANE Select	ENSP00000366326.4:n.153+135_153+136del
ENST00000674540.1:n.440+135_440+136del
ENST00000675114.1:n.565+64849_565+64850del
ENST00000675700.1:n.380+64849_380+64850del
ENST00000675702.1:n.636+64849_636+64850del
ENST00000675747.1:n.2515+135_2515+136del
ENST00000377119.5:n.163+135_163+136del
ENST00000377122.8:c.153+135_153+136del	ENSP00000366326.4:n.153+135_153+136del
ENST00000417816.2:c.357+64849_357+64850del	ENSP00000393896.2:n.357+64849_357+64850del
ENST00000434381.1:c.105+135_105+136del	ENSP00000396512.1:n.105+135_105+136del
NM_001173484.1:c.357+64849_357+64850del	NP_001166955.1:n.357+64849_357+64850del
NM_006393.2:c.153+135_153+136del , LRG_411t2:c.153+135_153+136del	NP_006384.1:n.153+135_153+136del
NM_213569.2:c.357+64849_357+64850del , LRG_411t1:c.357+64849_357+64850del	NP_998734.1:n.357+64849_357+64850del
XM_005252342.3:c.153+135_153+136del	XP_005252399.1:n.153+135_153+136del
XM_005252343.3:c.153+135_153+136del	XP_005252400.1:n.153+135_153+136del
XM_005252344.3:c.153+135_153+136del	XP_005252401.1:n.153+135_153+136del
XM_011519290.1:c.105+135_105+136del	XP_011517592.1:n.105+135_105+136del
XM_011519291.1:c.105+135_105+136del	XP_011517593.1:n.105+135_105+136del
XR_242691.3:n.265+135_265+136del
XM_005252342.5:c.153+135_153+136del	XP_005252399.1:n.153+135_153+136del
XM_005252343.5:c.153+135_153+136del	XP_005252400.1:n.153+135_153+136del
XM_005252344.5:c.153+135_153+136del	XP_005252401.1:n.153+135_153+136del
XM_011519291.2:c.105+135_105+136del	XP_011517593.1:n.105+135_105+136del
XM_017015468.1:c.105+135_105+136del	XP_016870957.1:n.105+135_105+136del
XR_001746995.2:n.1749+135_1749+136del
XR_001746996.1:n.468+135_468+136del
XR_242691.5:n.1749+135_1749+136del
NM_001173484.2:c.357+64849_357+64850del	NP_001166955.1:n.357+64849_357+64850del
NM_001377322.1:c.357+64849_357+64850del	NP_001364251.1:n.357+64849_357+64850del
NM_001377323.1:c.309+64849_309+64850del	NP_001364252.1:n.309+64849_309+64850del
NM_001377324.1:c.300+64849_300+64850del	NP_001364253.1:n.300+64849_300+64850del
NM_001377325.1:c.291+64849_291+64850del	NP_001364254.1:n.291+64849_291+64850del
NM_001377326.1:c.249+64849_249+64850del	NP_001364255.1:n.249+64849_249+64850del
NM_001377327.1:c.249+64849_249+64850del	NP_001364256.1:n.249+64849_249+64850del
NM_001377328.1:c.249+64849_249+64850del	NP_001364257.1:n.249+64849_249+64850del
NM_006393.3:c.153+135_153+136del MANE Select	NP_006384.1:n.153+135_153+136del