Canonical Allele Identifier: CA1329084834

Gene: NHEJ1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219157213A= , CM000664.2:g.219157213A=	GRCh38
NC_000002.11:g.220021935A= , CM000664.1:g.220021935A=	GRCh37
NC_000002.10:g.219730179A=	NCBI36
NG_007880.1:g.8653T= , LRG_90:g.8653T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426304.6:c.390+259T=	ENSP00000394896.2:n.390+259T=
ENST00000457600.3:c.390+259T=	ENSP00000407201.2:n.390+259T=
ENST00000698174.1:c.390+259T=	ENSP00000513594.1:n.390+259T=
ENST00000698175.1:c.*137+259T=	ENSP00000513595.1:n.*137+259T=
ENST00000698176.1:n.462+259T=
ENST00000698202.1:c.390+259T=	ENSP00000513605.1:n.390+259T=
ENST00000698203.1:c.390+259T=	ENSP00000513606.1:n.390+259T=
ENST00000356853.10:c.390+259T= MANE Select	ENSP00000349313.5:n.390+259T=
ENST00000318673.6:c.*1512+259T=	ENSP00000320919.3:n.*1512+259T=
ENST00000356853.9:c.390+259T=	ENSP00000349313.5:n.390+259T=
ENST00000409720.5:c.390+259T=	ENSP00000387290.1:n.390+259T=
ENST00000418099.5:c.390+259T=	ENSP00000408966.1:n.390+259T=
ENST00000426304.5:c.150+259T=	ENSP00000394896.1:n.150+259T=
ENST00000450447.1:c.*77+259T=	ENSP00000408421.1:n.*77+259T=
ENST00000457600.2:c.390+259T=	ENSP00000407201.1:n.390+259T=
ENST00000498327.5:n.2578+259T=
NM_024782.2:c.390+259T= , LRG_90t1:c.390+259T=	NP_079058.1:n.390+259T=
NM_001377498.1:c.390+259T=	NP_001364427.1:n.390+259T=
NM_001377499.1:c.390+259T=	NP_001364428.1:n.390+259T=
NM_024782.3:c.390+259T= MANE Select	NP_079058.1:n.390+259T=
NR_165304.1:n.486+259T=