Canonical Allele Identifier: CA1329079890
Gene: NHEJ1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219146685T= , CM000664.2:g.219146685T= GRCh38
NC_000002.11:g.220011407T= , CM000664.1:g.220011407T= GRCh37
NC_000002.10:g.219719651T= NCBI36
NG_007880.1:g.19181A= , LRG_90:g.19181A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000426304.6:c.583A= ENSP00000394896.2:p.Ile195=
ENST00000457600.3:c.583A= ENSP00000407201.2:p.Ile195=
ENST00000698174.1:c.583A= ENSP00000513594.1:p.Ile195=
ENST00000698175.1:c.*330A= ENSP00000513595.1:n.*330A=
ENST00000698176.1:n.655A=
ENST00000698202.1:c.583A= ENSP00000513605.1:p.Ile195=
ENST00000698203.1:c.583A= ENSP00000513606.1:p.Ile195=
ENST00000356853.10:c.583A= MANE Select ENSP00000349313.5:p.Ile195=
ENST00000318673.6:c.*1705A= ENSP00000320919.3:n.*1705A=
ENST00000356853.9:c.583A= ENSP00000349313.5:p.Ile195=
ENST00000409720.5:c.583A= ENSP00000387290.1:p.Ile195=
ENST00000418099.5:c.583A= ENSP00000408966.1:p.Ile195=
ENST00000426304.5:c.343A= ENSP00000394896.1:p.Ile115=
ENST00000457600.2:c.583A= ENSP00000407201.1:p.Ile195=
ENST00000498327.5:n.2771A=
NM_024782.2:c.583A= , LRG_90t1:c.583A= NP_079058.1:p.Ile195=
NM_001377498.1:c.583A= NP_001364427.1:p.Ile195=
NM_001377499.1:c.583A= NP_001364428.1:p.Ile195=
NM_024782.3:c.583A= MANE Select NP_079058.1:p.Ile195=
NR_165304.1:n.679A=