Canonical Allele Identifier: CA350633746

Gene: NHEJ1

Linked Data

• dbSNP Id: rs118204451
• gnomAD v2: 2-220022916-G-A
• gnomAD v4: 2-219158194-G-A
• MyVariant Identifiers: chr2:g.220022916G>A (hg19) ; chr2:g.219158194G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219158194G>A , CM000664.2:g.219158194G>A	GRCh38
NC_000002.11:g.220022916G>A , CM000664.1:g.220022916G>A	GRCh37
NC_000002.10:g.219731160G>A	NCBI36
NG_007880.1:g.7672C>T , LRG_90:g.7672C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000426304.6:c.169C>T	ENSP00000394896.2:p.Arg57Ter
ENST00000457600.3:c.169C>T	ENSP00000407201.2:p.Arg57Ter
ENST00000698174.1:c.169C>T	ENSP00000513594.1:p.Arg57Ter
ENST00000698175.1:c.169C>T	ENSP00000513595.1:p.Arg57Ter
ENST00000698176.1:n.241C>T
ENST00000698202.1:c.169C>T	ENSP00000513605.1:p.Arg57Ter
ENST00000698203.1:c.169C>T	ENSP00000513606.1:p.Arg57Ter
ENST00000356853.10:c.169C>T MANE Select	ENSP00000349313.5:p.Arg57Ter
ENST00000318673.6:c.*1291C>T	ENSP00000320919.3:n.*1291C>T
ENST00000356853.9:c.169C>T	ENSP00000349313.5:p.Arg57Ter
ENST00000409720.5:c.169C>T	ENSP00000387290.1:p.Arg57Ter
ENST00000418099.5:c.169C>T	ENSP00000408966.1:p.Arg57Ter
ENST00000450447.1:c.144+25C>T	ENSP00000408421.1:n.144+25C>T
ENST00000457600.2:c.169C>T	ENSP00000407201.1:p.Arg57Ter
ENST00000498327.5:n.2357C>T
NM_024782.2:c.169C>T , LRG_90t1:c.169C>T	NP_079058.1:p.Arg57Ter
NM_001377498.1:c.169C>T	NP_001364427.1:p.Arg57Ter
NM_001377499.1:c.169C>T	NP_001364428.1:p.Arg57Ter
NM_024782.3:c.169C>T MANE Select	NP_079058.1:p.Arg57Ter
NR_165304.1:n.265C>T