Canonical Allele Identifier: CA1801505094

Gene: NBN

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.89970362A= , CM000670.2:g.89970362A=	GRCh38
NC_000008.10:g.90982590A= , CM000670.1:g.90982590A=	GRCh37
NC_000008.9:g.91051766A=	NCBI36
NG_008860.1:g.19310T= , LRG_158:g.19310T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000494804.2:n.2198+2T=
ENST00000517337.2:c.650+2T=	ENSP00000429971.2:n.650+2T=
ENST00000523444.2:c.650+2T=	ENSP00000428252.2:n.650+2T=
ENST00000697292.1:c.896+2T=	ENSP00000513229.1:n.896+2T=
ENST00000697293.1:c.896+2T=	ENSP00000513230.1:n.896+2T=
ENST00000697294.1:c.*507+2T=	ENSP00000513231.1:n.*507+2T=
ENST00000697295.1:c.*205+2T=	ENSP00000513232.1:n.*205+2T=
ENST00000697296.1:c.*564+2T=	ENSP00000513233.1:n.*564+2T=
ENST00000697297.1:n.2681+2T=
ENST00000697298.1:c.650+2T=	ENSP00000513234.1:n.650+2T=
ENST00000697299.1:c.650+2T=	ENSP00000513235.1:n.650+2T=
ENST00000697300.1:c.*500+2T=	ENSP00000513236.1:n.*500+2T=
ENST00000697301.1:c.*417+2T=	ENSP00000513237.1:n.*417+2T=
ENST00000697302.1:c.*417+2T=	ENSP00000513238.1:n.*417+2T=
ENST00000697303.1:c.*500+2T=	ENSP00000513239.1:n.*500+2T=
ENST00000697304.1:c.585-5855T=	ENSP00000513240.1:n.585-5855T=
ENST00000697306.1:c.480+10372T=	ENSP00000513241.1:n.480+10372T=
ENST00000697307.1:c.896+2T=	ENSP00000513242.1:n.896+2T=
ENST00000697308.1:c.896+2T=	ENSP00000513243.1:n.896+2T=
ENST00000697309.1:c.896+2T=	ENSP00000513244.1:n.896+2T=
ENST00000697310.1:c.896+2T=	ENSP00000513245.1:n.896+2T=
ENST00000697311.1:c.896+2T=	ENSP00000513246.1:n.896+2T=
ENST00000697312.1:c.*294+2T=	ENSP00000513247.1:n.*294+2T=
ENST00000697313.1:n.2687+2T=
ENST00000697314.1:n.2687+2T=
ENST00000697315.1:c.896+2T=	ENSP00000513248.1:n.896+2T=
ENST00000697316.1:n.1017+2T=
ENST00000697317.1:n.1006+2T=
ENST00000697318.1:n.1008+2T=
ENST00000265433.8:c.896+2T= MANE Select	ENSP00000265433.4:n.896+2T=
ENST00000265433.7:c.896+2T=	ENSP00000265433.3:n.896+2T=
ENST00000396252.6:c.*769+2T=	ENSP00000379551.2:n.*769+2T=
ENST00000409330.5:c.650+2T=	ENSP00000386924.1:n.650+2T=
NM_001024688.2:c.650+2T=	NP_001019859.1:n.650+2T=
NM_002485.4:c.896+2T= , LRG_158t1:c.896+2T=	NP_002476.2:n.896+2T=
XM_011517044.1:c.872+2T=	XP_011515346.1:n.872+2T=
XM_011517045.1:c.650+2T=	XP_011515347.1:n.650+2T=
XM_011517046.1:c.896+2T=	XP_011515348.1:n.896+2T=
XR_928335.1:n.1033+2T=
XM_017013460.1:c.17+2T=	XP_016868949.1:n.17+2T=
XM_017013462.2:c.17+2T=	XP_016868951.1:n.17+2T=
XM_024447163.1:c.650+2T=	XP_024302931.1:n.650+2T=
XM_024447164.1:c.650+2T=	XP_024302932.1:n.650+2T=
XM_024447165.1:c.17+2T=	XP_024302933.1:n.17+2T=
NM_002485.5:c.896+2T= MANE Select	NP_002476.2:n.896+2T=
NM_001024688.3:c.650+2T=	NP_001019859.1:n.650+2T=