Canonical Allele Identifier: CA11172153
Gene: NHEJ1 HGNC NCBI

Linked Data

dbSNP Id: rs6724465
gnomAD v2: 2-219943846-G-A
gnomAD v3: 2-219079124-G-A
gnomAD v4: 2-219079124-G-A
MyVariant Identifiers: chr2:g.219943846G>A (hg19) chr2:g.219079124G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219079124G>A , CM000664.2:g.219079124G>A GRCh38
NC_000002.11:g.219943846G>A , CM000664.1:g.219943846G>A GRCh37
NC_000002.10:g.219652090G>A NCBI36
NG_007880.1:g.86742C>T , LRG_90:g.86742C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000426304.6:c.589-918C>T ENSP00000394896.2:n.589-918C>T
ENST00000457600.3:c.589-918C>T ENSP00000407201.2:n.589-918C>T
ENST00000698174.1:c.589-918C>T ENSP00000513594.1:n.589-918C>T
ENST00000698175.1:c.*336-918C>T ENSP00000513595.1:n.*336-918C>T
ENST00000698176.1:n.661-918C>T
ENST00000698202.1:c.589-918C>T ENSP00000513605.1:n.589-918C>T
ENST00000698203.1:c.589-918C>T ENSP00000513606.1:n.589-918C>T
ENST00000356853.10:c.589-918C>T MANE Select ENSP00000349313.5:n.589-918C>T
ENST00000318673.6:c.*1711-918C>T ENSP00000320919.3:n.*1711-918C>T
ENST00000356853.9:c.589-918C>T ENSP00000349313.5:n.589-918C>T
ENST00000409720.5:c.589-918C>T ENSP00000387290.1:n.589-918C>T
ENST00000418099.5:c.671-918C>T ENSP00000408966.1:n.671-918C>T
ENST00000426304.5:c.349-918C>T ENSP00000394896.1:n.349-918C>T
ENST00000457600.2:c.589-918C>T ENSP00000407201.1:n.589-918C>T
ENST00000483627.1:n.273-918C>T
ENST00000491159.5:n.183-918C>T
ENST00000494211.5:n.155-918C>T
ENST00000498327.5:n.2859-918C>T
NM_024782.2:c.589-918C>T , LRG_90t1:c.589-918C>T NP_079058.1:n.589-918C>T
NM_001377498.1:c.589-918C>T NP_001364427.1:n.589-918C>T
NM_001377499.1:c.589-918C>T NP_001364428.1:n.589-918C>T
NM_024782.3:c.589-918C>T MANE Select NP_079058.1:n.589-918C>T
NR_165304.1:n.767-918C>T
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