Canonical Allele Identifier: CA1895553583
Gene: NEBL HGNC NCBI

Linked Data

dbSNP Id: rs1839937398

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.21147295_21147297dup , CM000672.2:g.21147295_21147297dup GRCh38
NC_000010.10:g.21436224_21436226dup , CM000672.1:g.21436224_21436226dup GRCh37
NC_000010.9:g.21476230_21476232dup NCBI36
NG_017092.1:g.31892_31894dup , LRG_411:g.31892_31894dup

Transcript Alleles

HGVS Amino-acid change
ENST00000675700.1:n.187+25087_187+25089dup
ENST00000675702.1:n.443+25087_443+25089dup
ENST00000675747.1:n.224+25087_224+25089dup
ENST00000417816.2:c.164+25087_164+25089dup ENSP00000393896.2:n.164+25087_164+25089dup
NM_001173484.1:c.164+25087_164+25089dup NP_001166955.1:n.164+25087_164+25089dup
NM_213569.2:c.164+25087_164+25089dup , LRG_411t1:c.164+25087_164+25089dup NP_998734.1:n.164+25087_164+25089dup
NM_001173484.2:c.164+25087_164+25089dup NP_001166955.1:n.164+25087_164+25089dup
NM_001377322.1:c.164+25087_164+25089dup NP_001364251.1:n.164+25087_164+25089dup
NM_001377323.1:c.116+25087_116+25089dup NP_001364252.1:n.116+25087_116+25089dup
NM_001377324.1:c.107+25087_107+25089dup NP_001364253.1:n.107+25087_107+25089dup
NM_001377325.1:c.98+25087_98+25089dup NP_001364254.1:n.98+25087_98+25089dup
NM_001377326.1:c.56+25087_56+25089dup NP_001364255.1:n.56+25087_56+25089dup
NM_001377327.1:c.56+25087_56+25089dup NP_001364256.1:n.56+25087_56+25089dup
NM_001377328.1:c.56+25087_56+25089dup NP_001364257.1:n.56+25087_56+25089dup