Canonical Allele Identifier: CA350626674
Gene: NHEJ1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219146682C>A , CM000664.2:g.219146682C>A GRCh38
NC_000002.11:g.220011404C>A , CM000664.1:g.220011404C>A GRCh37
NC_000002.10:g.219719648C>A NCBI36
NG_007880.1:g.19184G>T , LRG_90:g.19184G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000426304.6:c.586G>T ENSP00000394896.2:p.Glu196Ter
ENST00000457600.3:c.586G>T ENSP00000407201.2:p.Glu196Ter
ENST00000698174.1:c.586G>T ENSP00000513594.1:p.Glu196Ter
ENST00000698175.1:c.*333G>T ENSP00000513595.1:n.*333G>T
ENST00000698176.1:n.658G>T
ENST00000698202.1:c.586G>T ENSP00000513605.1:p.Glu196Ter
ENST00000698203.1:c.586G>T ENSP00000513606.1:p.Glu196Ter
ENST00000356853.10:c.586G>T MANE Select ENSP00000349313.5:p.Glu196Ter
ENST00000318673.6:c.*1708G>T ENSP00000320919.3:n.*1708G>T
ENST00000356853.9:c.586G>T ENSP00000349313.5:p.Glu196Ter
ENST00000409720.5:c.586G>T ENSP00000387290.1:p.Glu196Ter
ENST00000418099.5:c.586G>T ENSP00000408966.1:p.Glu196Ter
ENST00000426304.5:c.346G>T ENSP00000394896.1:p.Glu116Ter
ENST00000457600.2:c.586G>T ENSP00000407201.1:p.Glu196Ter
ENST00000498327.5:n.2774G>T
NM_024782.2:c.586G>T , LRG_90t1:c.586G>T NP_079058.1:p.Glu196Ter
NM_001377498.1:c.586G>T NP_001364427.1:p.Glu196Ter
NM_001377499.1:c.586G>T NP_001364428.1:p.Glu196Ter
NM_024782.3:c.586G>T MANE Select NP_079058.1:p.Glu196Ter
NR_165304.1:n.682G>T