Canonical Allele Identifier: CA376098720

Gene: NEBL

Linked Data

• gnomAD v4: 10-20897009-A-C
• MyVariant Identifiers: chr10:g.21185938A>C (hg19) ; chr10:g.20897009A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.20897009A>C , CM000672.2:g.20897009A>C	GRCh38
NC_000010.10:g.21185938A>C , CM000672.1:g.21185938A>C	GRCh37
NC_000010.9:g.21225944A>C	NCBI36
NG_017092.1:g.282179T>G , LRG_411:g.282179T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377122.9:c.102T>G MANE Select	ENSP00000366326.4:p.Ile34Met
ENST00000674540.1:n.389T>G
ENST00000675114.1:n.565+64663T>G
ENST00000675700.1:n.380+64663T>G
ENST00000675702.1:n.636+64663T>G
ENST00000675747.1:n.2464T>G
ENST00000377119.5:n.112T>G
ENST00000377122.8:c.102T>G	ENSP00000366326.4:p.Ile34Met
ENST00000417816.2:c.357+64663T>G	ENSP00000393896.2:n.357+64663T>G
ENST00000434381.1:c.54T>G	ENSP00000396512.1:p.Ile18Met
NM_001173484.1:c.357+64663T>G	NP_001166955.1:n.357+64663T>G
NM_006393.2:c.102T>G , LRG_411t2:c.102T>G	NP_006384.1:p.Ile34Met
NM_213569.2:c.357+64663T>G , LRG_411t1:c.357+64663T>G	NP_998734.1:n.357+64663T>G
XM_005252342.3:c.102T>G	XP_005252399.1:p.Ile34Met
XM_005252343.3:c.102T>G	XP_005252400.1:p.Ile34Met
XM_005252344.3:c.102T>G	XP_005252401.1:p.Ile34Met
XM_011519290.1:c.54T>G	XP_011517592.1:p.Ile18Met
XM_011519291.1:c.54T>G	XP_011517593.1:p.Ile18Met
XR_242691.3:n.214T>G
XM_005252342.5:c.102T>G	XP_005252399.1:p.Ile34Met
XM_005252343.5:c.102T>G	XP_005252400.1:p.Ile34Met
XM_005252344.5:c.102T>G	XP_005252401.1:p.Ile34Met
XM_011519291.2:c.54T>G	XP_011517593.1:p.Ile18Met
XM_017015468.1:c.54T>G	XP_016870957.1:p.Ile18Met
XR_001746995.2:n.1698T>G
XR_001746996.1:n.417T>G
XR_242691.5:n.1698T>G
NM_001173484.2:c.357+64663T>G	NP_001166955.1:n.357+64663T>G
NM_001377322.1:c.357+64663T>G	NP_001364251.1:n.357+64663T>G
NM_001377323.1:c.309+64663T>G	NP_001364252.1:n.309+64663T>G
NM_001377324.1:c.300+64663T>G	NP_001364253.1:n.300+64663T>G
NM_001377325.1:c.291+64663T>G	NP_001364254.1:n.291+64663T>G
NM_001377326.1:c.249+64663T>G	NP_001364255.1:n.249+64663T>G
NM_001377327.1:c.249+64663T>G	NP_001364256.1:n.249+64663T>G
NM_001377328.1:c.249+64663T>G	NP_001364257.1:n.249+64663T>G
NM_006393.3:c.102T>G MANE Select	NP_006384.1:p.Ile34Met