Canonical Allele Identifier: CA350626781
Gene: NHEJ1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219146706A>T , CM000664.2:g.219146706A>T GRCh38
NC_000002.11:g.220011428A>T , CM000664.1:g.220011428A>T GRCh37
NC_000002.10:g.219719672A>T NCBI36
NG_007880.1:g.19160T>A , LRG_90:g.19160T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000426304.6:c.562T>A ENSP00000394896.2:p.Ser188Thr
ENST00000457600.3:c.562T>A ENSP00000407201.2:p.Ser188Thr
ENST00000698174.1:c.562T>A ENSP00000513594.1:p.Ser188Thr
ENST00000698175.1:c.*309T>A ENSP00000513595.1:n.*309T>A
ENST00000698176.1:n.634T>A
ENST00000698202.1:c.562T>A ENSP00000513605.1:p.Ser188Thr
ENST00000698203.1:c.562T>A ENSP00000513606.1:p.Ser188Thr
ENST00000356853.10:c.562T>A MANE Select ENSP00000349313.5:p.Ser188Thr
ENST00000318673.6:c.*1684T>A ENSP00000320919.3:n.*1684T>A
ENST00000356853.9:c.562T>A ENSP00000349313.5:p.Ser188Thr
ENST00000409720.5:c.562T>A ENSP00000387290.1:p.Ser188Thr
ENST00000418099.5:c.562T>A ENSP00000408966.1:p.Ser188Thr
ENST00000426304.5:c.322T>A ENSP00000394896.1:p.Ser108Thr
ENST00000457600.2:c.562T>A ENSP00000407201.1:p.Ser188Thr
ENST00000498327.5:n.2750T>A
NM_024782.2:c.562T>A , LRG_90t1:c.562T>A NP_079058.1:p.Ser188Thr
NM_001377498.1:c.562T>A NP_001364427.1:p.Ser188Thr
NM_001377499.1:c.562T>A NP_001364428.1:p.Ser188Thr
NM_024782.3:c.562T>A MANE Select NP_079058.1:p.Ser188Thr
NR_165304.1:n.658T>A