Canonical Allele Identifier: CA1329079867
Gene: NHEJ1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219146638G= , CM000664.2:g.219146638G= GRCh38
NC_000002.11:g.220011360G= , CM000664.1:g.220011360G= GRCh37
NC_000002.10:g.219719604G= NCBI36
NG_007880.1:g.19228C= , LRG_90:g.19228C=

Transcript Alleles

HGVS Amino-acid change
ENST00000426304.6:c.588+42C= ENSP00000394896.2:n.588+42C=
ENST00000457600.3:c.588+42C= ENSP00000407201.2:n.588+42C=
ENST00000698174.1:c.588+42C= ENSP00000513594.1:n.588+42C=
ENST00000698175.1:c.*335+42C= ENSP00000513595.1:n.*335+42C=
ENST00000698176.1:n.660+42C=
ENST00000698202.1:c.588+42C= ENSP00000513605.1:n.588+42C=
ENST00000698203.1:c.588+42C= ENSP00000513606.1:n.588+42C=
ENST00000356853.10:c.588+42C= MANE Select ENSP00000349313.5:n.588+42C=
ENST00000318673.6:c.*1710+42C= ENSP00000320919.3:n.*1710+42C=
ENST00000356853.9:c.588+42C= ENSP00000349313.5:n.588+42C=
ENST00000409720.5:c.588+42C= ENSP00000387290.1:n.588+42C=
ENST00000418099.5:c.588+42C= ENSP00000408966.1:n.588+42C=
ENST00000426304.5:c.348+42C= ENSP00000394896.1:n.348+42C=
ENST00000457600.2:c.588+42C= ENSP00000407201.1:n.588+42C=
ENST00000498327.5:n.2776+42C=
NM_024782.2:c.588+42C= , LRG_90t1:c.588+42C= NP_079058.1:n.588+42C=
NM_001377498.1:c.588+42C= NP_001364427.1:n.588+42C=
NM_001377499.1:c.588+42C= NP_001364428.1:n.588+42C=
NM_024782.3:c.588+42C= MANE Select NP_079058.1:n.588+42C=
NR_165304.1:n.684+42C=