Canonical Allele Identifier: CA1329079891

Gene: NHEJ1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219146686C= , CM000664.2:g.219146686C=	GRCh38
NC_000002.11:g.220011408C= , CM000664.1:g.220011408C=	GRCh37
NC_000002.10:g.219719652C=	NCBI36
NG_007880.1:g.19180G= , LRG_90:g.19180G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426304.6:c.582G=	ENSP00000394896.2:p.Met194=
ENST00000457600.3:c.582G=	ENSP00000407201.2:p.Met194=
ENST00000698174.1:c.582G=	ENSP00000513594.1:p.Met194=
ENST00000698175.1:c.*329G=	ENSP00000513595.1:n.*329G=
ENST00000698176.1:n.654G=
ENST00000698202.1:c.582G=	ENSP00000513605.1:p.Met194=
ENST00000698203.1:c.582G=	ENSP00000513606.1:p.Met194=
ENST00000356853.10:c.582G= MANE Select	ENSP00000349313.5:p.Met194=
ENST00000318673.6:c.*1704G=	ENSP00000320919.3:n.*1704G=
ENST00000356853.9:c.582G=	ENSP00000349313.5:p.Met194=
ENST00000409720.5:c.582G=	ENSP00000387290.1:p.Met194=
ENST00000418099.5:c.582G=	ENSP00000408966.1:p.Met194=
ENST00000426304.5:c.342G=	ENSP00000394896.1:p.Met114=
ENST00000457600.2:c.582G=	ENSP00000407201.1:p.Met194=
ENST00000498327.5:n.2770G=
NM_024782.2:c.582G= , LRG_90t1:c.582G=	NP_079058.1:p.Met194=
NM_001377498.1:c.582G=	NP_001364427.1:p.Met194=
NM_001377499.1:c.582G=	NP_001364428.1:p.Met194=
NM_024782.3:c.582G= MANE Select	NP_079058.1:p.Met194=
NR_165304.1:n.678G=