Canonical Allele Identifier: CA1329050795

Gene: NHEJ1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219079196C= , CM000664.2:g.219079196C=	GRCh38
NC_000002.11:g.219943918C= , CM000664.1:g.219943918C=	GRCh37
NC_000002.10:g.219652162C=	NCBI36
NG_007880.1:g.86670G= , LRG_90:g.86670G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426304.6:c.589-990G=	ENSP00000394896.2:n.589-990G=
ENST00000457600.3:c.589-990G=	ENSP00000407201.2:n.589-990G=
ENST00000698174.1:c.589-990G=	ENSP00000513594.1:n.589-990G=
ENST00000698175.1:c.*336-990G=	ENSP00000513595.1:n.*336-990G=
ENST00000698176.1:n.661-990G=
ENST00000698202.1:c.589-990G=	ENSP00000513605.1:n.589-990G=
ENST00000698203.1:c.589-990G=	ENSP00000513606.1:n.589-990G=
ENST00000356853.10:c.589-990G= MANE Select	ENSP00000349313.5:n.589-990G=
ENST00000318673.6:c.*1711-990G=	ENSP00000320919.3:n.*1711-990G=
ENST00000356853.9:c.589-990G=	ENSP00000349313.5:n.589-990G=
ENST00000409720.5:c.589-990G=	ENSP00000387290.1:n.589-990G=
ENST00000418099.5:c.671-990G=	ENSP00000408966.1:n.671-990G=
ENST00000426304.5:c.349-990G=	ENSP00000394896.1:n.349-990G=
ENST00000457600.2:c.589-990G=	ENSP00000407201.1:n.589-990G=
ENST00000483627.1:n.273-990G=
ENST00000491159.5:n.183-990G=
ENST00000494211.5:n.155-990G=
ENST00000498327.5:n.2859-990G=
NM_024782.2:c.589-990G= , LRG_90t1:c.589-990G=	NP_079058.1:n.589-990G=
NM_001377498.1:c.589-990G=	NP_001364427.1:n.589-990G=
NM_001377499.1:c.589-990G=	NP_001364428.1:n.589-990G=
NM_024782.3:c.589-990G= MANE Select	NP_079058.1:n.589-990G=
NR_165304.1:n.767-990G=