Canonical Allele Identifier: CA1329079920
Gene: NHEJ1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219146753A= , CM000664.2:g.219146753A= GRCh38
NC_000002.11:g.220011475A= , CM000664.1:g.220011475A= GRCh37
NC_000002.10:g.219719719A= NCBI36
NG_007880.1:g.19113T= , LRG_90:g.19113T=

Transcript Alleles

HGVS Amino-acid change
ENST00000426304.6:c.530-15T= ENSP00000394896.2:n.530-15T=
ENST00000457600.3:c.530-15T= ENSP00000407201.2:n.530-15T=
ENST00000698174.1:c.530-15T= ENSP00000513594.1:n.530-15T=
ENST00000698175.1:c.*277-15T= ENSP00000513595.1:n.*277-15T=
ENST00000698176.1:n.602-15T=
ENST00000698202.1:c.530-15T= ENSP00000513605.1:n.530-15T=
ENST00000698203.1:c.530-15T= ENSP00000513606.1:n.530-15T=
ENST00000356853.10:c.530-15T= MANE Select ENSP00000349313.5:n.530-15T=
ENST00000318673.6:c.*1652-15T= ENSP00000320919.3:n.*1652-15T=
ENST00000356853.9:c.530-15T= ENSP00000349313.5:n.530-15T=
ENST00000409720.5:c.530-15T= ENSP00000387290.1:n.530-15T=
ENST00000418099.5:c.530-15T= ENSP00000408966.1:n.530-15T=
ENST00000426304.5:c.290-15T= ENSP00000394896.1:n.290-15T=
ENST00000450447.1:c.*217-15T= ENSP00000408421.1:n.*217-15T=
ENST00000457600.2:c.530-15T= ENSP00000407201.1:n.530-15T=
ENST00000498327.5:n.2718-15T=
NM_024782.2:c.530-15T= , LRG_90t1:c.530-15T= NP_079058.1:n.530-15T=
NM_001377498.1:c.530-15T= NP_001364427.1:n.530-15T=
NM_001377499.1:c.530-15T= NP_001364428.1:n.530-15T=
NM_024782.3:c.530-15T= MANE Select NP_079058.1:n.530-15T=
NR_165304.1:n.626-15T=