Canonical Allele Identifier: CA764943903

Gene: NHEJ1

Linked Data

• dbSNP Id: rs1471779362
• MyVariant Identifiers: chr2:g.219943946A>G (hg19) ; chr2:g.219079224A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219079224A>G , CM000664.2:g.219079224A>G	GRCh38
NC_000002.11:g.219943946A>G , CM000664.1:g.219943946A>G	GRCh37
NC_000002.10:g.219652190A>G	NCBI36
NG_007880.1:g.86642T>C , LRG_90:g.86642T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426304.6:c.589-1018T>C	ENSP00000394896.2:n.589-1018T>C
ENST00000457600.3:c.589-1018T>C	ENSP00000407201.2:n.589-1018T>C
ENST00000698174.1:c.589-1018T>C	ENSP00000513594.1:n.589-1018T>C
ENST00000698175.1:c.*336-1018T>C	ENSP00000513595.1:n.*336-1018T>C
ENST00000698176.1:n.661-1018T>C
ENST00000698202.1:c.589-1018T>C	ENSP00000513605.1:n.589-1018T>C
ENST00000698203.1:c.589-1018T>C	ENSP00000513606.1:n.589-1018T>C
ENST00000356853.10:c.589-1018T>C MANE Select	ENSP00000349313.5:n.589-1018T>C
ENST00000318673.6:c.*1711-1018T>C	ENSP00000320919.3:n.*1711-1018T>C
ENST00000356853.9:c.589-1018T>C	ENSP00000349313.5:n.589-1018T>C
ENST00000409720.5:c.589-1018T>C	ENSP00000387290.1:n.589-1018T>C
ENST00000418099.5:c.671-1018T>C	ENSP00000408966.1:n.671-1018T>C
ENST00000426304.5:c.349-1018T>C	ENSP00000394896.1:n.349-1018T>C
ENST00000457600.2:c.589-1018T>C	ENSP00000407201.1:n.589-1018T>C
ENST00000483627.1:n.273-1018T>C
ENST00000491159.5:n.183-1018T>C
ENST00000494211.5:n.155-1018T>C
ENST00000498327.5:n.2859-1018T>C
NM_024782.2:c.589-1018T>C , LRG_90t1:c.589-1018T>C	NP_079058.1:n.589-1018T>C
NM_001377498.1:c.589-1018T>C	NP_001364427.1:n.589-1018T>C
NM_001377499.1:c.589-1018T>C	NP_001364428.1:n.589-1018T>C
NM_024782.3:c.589-1018T>C MANE Select	NP_079058.1:n.589-1018T>C
NR_165304.1:n.767-1018T>C