Canonical Allele Identifier: CA1329084974

Gene: NHEJ1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219157514G= , CM000664.2:g.219157514G=	GRCh38
NC_000002.11:g.220022236G= , CM000664.1:g.220022236G=	GRCh37
NC_000002.10:g.219730480G=	NCBI36
NG_007880.1:g.8352C= , LRG_90:g.8352C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426304.6:c.348C=	ENSP00000394896.2:p.Pro116=
ENST00000457600.3:c.348C=	ENSP00000407201.2:p.Pro116=
ENST00000698174.1:c.348C=	ENSP00000513594.1:p.Pro116=
ENST00000698175.1:c.*95C=	ENSP00000513595.1:n.*95C=
ENST00000698176.1:n.420C=
ENST00000698202.1:c.348C=	ENSP00000513605.1:p.Pro116=
ENST00000698203.1:c.348C=	ENSP00000513606.1:p.Pro116=
ENST00000356853.10:c.348C= MANE Select	ENSP00000349313.5:p.Pro116=
ENST00000318673.6:c.*1470C=	ENSP00000320919.3:n.*1470C=
ENST00000356853.9:c.348C=	ENSP00000349313.5:p.Pro116=
ENST00000409720.5:c.348C=	ENSP00000387290.1:p.Pro116=
ENST00000418099.5:c.348C=	ENSP00000408966.1:p.Pro116=
ENST00000426304.5:c.108C=	ENSP00000394896.1:p.Pro36=
ENST00000450447.1:c.*35C=	ENSP00000408421.1:n.*35C=
ENST00000457600.2:c.348C=	ENSP00000407201.1:p.Pro116=
ENST00000498327.5:n.2536C=
NM_024782.2:c.348C= , LRG_90t1:c.348C=	NP_079058.1:p.Pro116=
NM_001377498.1:c.348C=	NP_001364427.1:p.Pro116=
NM_001377499.1:c.348C=	NP_001364428.1:p.Pro116=
NM_024782.3:c.348C= MANE Select	NP_079058.1:p.Pro116=
NR_165304.1:n.444C=