Canonical Allele Identifier: CA350626729

Gene: NHEJ1

Linked Data

• MyVariant Identifiers: chr2:g.220011416G>C (hg19) ; chr2:g.219146694G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219146694G>C , CM000664.2:g.219146694G>C	GRCh38
NC_000002.11:g.220011416G>C , CM000664.1:g.220011416G>C	GRCh37
NC_000002.10:g.219719660G>C	NCBI36
NG_007880.1:g.19172C>G , LRG_90:g.19172C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426304.6:c.574C>G	ENSP00000394896.2:p.Gln192Glu
ENST00000457600.3:c.574C>G	ENSP00000407201.2:p.Gln192Glu
ENST00000698174.1:c.574C>G	ENSP00000513594.1:p.Gln192Glu
ENST00000698175.1:c.*321C>G	ENSP00000513595.1:n.*321C>G
ENST00000698176.1:n.646C>G
ENST00000698202.1:c.574C>G	ENSP00000513605.1:p.Gln192Glu
ENST00000698203.1:c.574C>G	ENSP00000513606.1:p.Gln192Glu
ENST00000356853.10:c.574C>G MANE Select	ENSP00000349313.5:p.Gln192Glu
ENST00000318673.6:c.*1696C>G	ENSP00000320919.3:n.*1696C>G
ENST00000356853.9:c.574C>G	ENSP00000349313.5:p.Gln192Glu
ENST00000409720.5:c.574C>G	ENSP00000387290.1:p.Gln192Glu
ENST00000418099.5:c.574C>G	ENSP00000408966.1:p.Gln192Glu
ENST00000426304.5:c.334C>G	ENSP00000394896.1:p.Gln112Glu
ENST00000457600.2:c.574C>G	ENSP00000407201.1:p.Gln192Glu
ENST00000498327.5:n.2762C>G
NM_024782.2:c.574C>G , LRG_90t1:c.574C>G	NP_079058.1:p.Gln192Glu
NM_001377498.1:c.574C>G	NP_001364427.1:p.Gln192Glu
NM_001377499.1:c.574C>G	NP_001364428.1:p.Gln192Glu
NM_024782.3:c.574C>G MANE Select	NP_079058.1:p.Gln192Glu
NR_165304.1:n.670C>G