Canonical Allele Identifier: CA350626829

Gene: NHEJ1

Linked Data

• MyVariant Identifiers: chr2:g.220011448G>A (hg19) ; chr2:g.219146726G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219146726G>A , CM000664.2:g.219146726G>A	GRCh38
NC_000002.11:g.220011448G>A , CM000664.1:g.220011448G>A	GRCh37
NC_000002.10:g.219719692G>A	NCBI36
NG_007880.1:g.19140C>T , LRG_90:g.19140C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426304.6:c.542C>T	ENSP00000394896.2:p.Thr181Ile
ENST00000457600.3:c.542C>T	ENSP00000407201.2:p.Thr181Ile
ENST00000698174.1:c.542C>T	ENSP00000513594.1:p.Thr181Ile
ENST00000698175.1:c.*289C>T	ENSP00000513595.1:n.*289C>T
ENST00000698176.1:n.614C>T
ENST00000698202.1:c.542C>T	ENSP00000513605.1:p.Thr181Ile
ENST00000698203.1:c.542C>T	ENSP00000513606.1:p.Thr181Ile
ENST00000356853.10:c.542C>T MANE Select	ENSP00000349313.5:p.Thr181Ile
ENST00000318673.6:c.*1664C>T	ENSP00000320919.3:n.*1664C>T
ENST00000356853.9:c.542C>T	ENSP00000349313.5:p.Thr181Ile
ENST00000409720.5:c.542C>T	ENSP00000387290.1:p.Thr181Ile
ENST00000418099.5:c.542C>T	ENSP00000408966.1:p.Thr181Ile
ENST00000426304.5:c.302C>T	ENSP00000394896.1:p.Thr101Ile
ENST00000450447.1:c.*229C>T	ENSP00000408421.1:n.*229C>T
ENST00000457600.2:c.542C>T	ENSP00000407201.1:p.Thr181Ile
ENST00000498327.5:n.2730C>T
NM_024782.2:c.542C>T , LRG_90t1:c.542C>T	NP_079058.1:p.Thr181Ile
NM_001377498.1:c.542C>T	NP_001364427.1:p.Thr181Ile
NM_001377499.1:c.542C>T	NP_001364428.1:p.Thr181Ile
NM_024782.3:c.542C>T MANE Select	NP_079058.1:p.Thr181Ile
NR_165304.1:n.638C>T