Canonical Allele Identifier: CA764937735
Gene: NHEJ1 HGNC NCBI

Linked Data

dbSNP Id: rs1227580559

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219147186_219147187del , CM000664.2:g.219147186_219147187del GRCh38
NC_000002.11:g.220011908_220011909del , CM000664.1:g.220011908_220011909del GRCh37
NC_000002.10:g.219720152_219720153del NCBI36
NG_007880.1:g.18681_18682del , LRG_90:g.18681_18682del

Transcript Alleles

HGVS Amino-acid Change
ENST00000426304.6:c.530-447_530-446del ENSP00000394896.2:n.530-447_530-446del
ENST00000457600.3:c.530-447_530-446del ENSP00000407201.2:n.530-447_530-446del
ENST00000698174.1:c.530-447_530-446del ENSP00000513594.1:n.530-447_530-446del
ENST00000698175.1:c.*277-447_*277-446del ENSP00000513595.1:n.*277-447_*277-446del
ENST00000698176.1:n.602-447_602-446del
ENST00000698202.1:c.530-447_530-446del ENSP00000513605.1:n.530-447_530-446del
ENST00000698203.1:c.530-447_530-446del ENSP00000513606.1:n.530-447_530-446del
ENST00000356853.10:c.530-447_530-446del MANE Select ENSP00000349313.5:n.530-447_530-446del
ENST00000318673.6:c.*1652-447_*1652-446del ENSP00000320919.3:n.*1652-447_*1652-446del
ENST00000356853.9:c.530-447_530-446del ENSP00000349313.5:n.530-447_530-446del
ENST00000409720.5:c.530-447_530-446del ENSP00000387290.1:n.530-447_530-446del
ENST00000418099.5:c.530-447_530-446del ENSP00000408966.1:n.530-447_530-446del
ENST00000426304.5:c.290-447_290-446del ENSP00000394896.1:n.290-447_290-446del
ENST00000450447.1:c.*217-447_*217-446del ENSP00000408421.1:n.*217-447_*217-446del
ENST00000457600.2:c.530-447_530-446del ENSP00000407201.1:n.530-447_530-446del
ENST00000498327.5:n.2718-447_2718-446del
NM_024782.2:c.530-447_530-446del , LRG_90t1:c.530-447_530-446del NP_079058.1:n.530-447_530-446del
NM_001377498.1:c.530-447_530-446del NP_001364427.1:n.530-447_530-446del
NM_001377499.1:c.530-447_530-446del NP_001364428.1:n.530-447_530-446del
NM_024782.3:c.530-447_530-446del MANE Select NP_079058.1:n.530-447_530-446del
NR_165304.1:n.626-447_626-446del