Canonical Allele Identifier: CA1895553598

Gene: NEBL

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.21147316_21147317delinsAG , CM000672.2:g.21147316_21147317delinsAG	GRCh38
NC_000010.10:g.21436245_21436246delinsAG , CM000672.1:g.21436245_21436246delinsAG	GRCh37
NC_000010.9:g.21476251_21476252delinsAG	NCBI36
NG_017092.1:g.31871_31872delinsCT , LRG_411:g.31871_31872delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000675700.1:n.187+25066_187+25067delinsCT
ENST00000675702.1:n.443+25066_443+25067delinsCT
ENST00000675747.1:n.224+25066_224+25067delinsCT
ENST00000417816.2:c.164+25066_164+25067delinsCT	ENSP00000393896.2:n.164+25066_164+25067delinsCT
NM_001173484.1:c.164+25066_164+25067delinsCT	NP_001166955.1:n.164+25066_164+25067delinsCT
NM_213569.2:c.164+25066_164+25067delinsCT , LRG_411t1:c.164+25066_164+25067delinsCT	NP_998734.1:n.164+25066_164+25067delinsCT
NM_001173484.2:c.164+25066_164+25067delinsCT	NP_001166955.1:n.164+25066_164+25067delinsCT
NM_001377322.1:c.164+25066_164+25067delinsCT	NP_001364251.1:n.164+25066_164+25067delinsCT
NM_001377323.1:c.116+25066_116+25067delinsCT	NP_001364252.1:n.116+25066_116+25067delinsCT
NM_001377324.1:c.107+25066_107+25067delinsCT	NP_001364253.1:n.107+25066_107+25067delinsCT
NM_001377325.1:c.98+25066_98+25067delinsCT	NP_001364254.1:n.98+25066_98+25067delinsCT
NM_001377326.1:c.56+25066_56+25067delinsCT	NP_001364255.1:n.56+25066_56+25067delinsCT
NM_001377327.1:c.56+25066_56+25067delinsCT	NP_001364256.1:n.56+25066_56+25067delinsCT
NM_001377328.1:c.56+25066_56+25067delinsCT	NP_001364257.1:n.56+25066_56+25067delinsCT