Canonical Allele Identifier: CA1801423139

Gene: NBN

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.89953917C= , CM000670.2:g.89953917C=	GRCh38
NC_000008.10:g.90966145C= , CM000670.1:g.90966145C=	GRCh37
NC_000008.9:g.91035321C=	NCBI36
NG_008860.1:g.35755G= , LRG_158:g.35755G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000494804.2:n.2700-226G=
ENST00000517337.2:c.1152-226G=	ENSP00000429971.2:n.1152-226G=
ENST00000523444.2:c.1152-226G=	ENSP00000428252.2:n.1152-226G=
ENST00000697292.1:c.1398-226G=	ENSP00000513229.1:n.1398-226G=
ENST00000697293.1:c.1398-226G=	ENSP00000513230.1:n.1398-226G=
ENST00000697294.1:c.*1009-226G=	ENSP00000513231.1:n.*1009-226G=
ENST00000697295.1:c.*707-226G=	ENSP00000513232.1:n.*707-226G=
ENST00000697296.1:c.*1066-226G=	ENSP00000513233.1:n.*1066-226G=
ENST00000697297.1:n.3183-226G=
ENST00000697298.1:c.1152-226G=	ENSP00000513234.1:n.1152-226G=
ENST00000697299.1:c.1152-226G=	ENSP00000513235.1:n.1152-226G=
ENST00000697300.1:c.*1002-226G=	ENSP00000513236.1:n.*1002-226G=
ENST00000697301.1:c.*919-226G=	ENSP00000513237.1:n.*919-226G=
ENST00000697302.1:c.*919-226G=	ENSP00000513238.1:n.*919-226G=
ENST00000697303.1:c.*1002-226G=	ENSP00000513239.1:n.*1002-226G=
ENST00000697304.1:c.1086-226G=	ENSP00000513240.1:n.1086-226G=
ENST00000697306.1:c.*398-226G=	ENSP00000513241.1:n.*398-226G=
ENST00000697307.1:c.1398-226G=	ENSP00000513242.1:n.1398-226G=
ENST00000697308.1:c.1398-226G=	ENSP00000513243.1:n.1398-226G=
ENST00000697309.1:c.1398-226G=	ENSP00000513244.1:n.1398-226G=
ENST00000697310.1:c.1398-226G=	ENSP00000513245.1:n.1398-226G=
ENST00000697311.1:c.1398-226G=	ENSP00000513246.1:n.1398-226G=
ENST00000697312.1:c.*796-226G=	ENSP00000513247.1:n.*796-226G=
ENST00000697313.1:n.2687+16447G=
ENST00000697314.1:n.3189-226G=
ENST00000697315.1:c.1398-226G=	ENSP00000513248.1:n.1398-226G=
ENST00000697316.1:n.1519-226G=
ENST00000697317.1:n.1508-226G=
ENST00000697318.1:n.1510-226G=
ENST00000265433.8:c.1398-226G= MANE Select	ENSP00000265433.4:n.1398-226G=
ENST00000265433.7:c.1398-226G=	ENSP00000265433.3:n.1398-226G=
ENST00000396252.6:c.*1271-226G=	ENSP00000379551.2:n.*1271-226G=
ENST00000409330.5:c.1152-226G=	ENSP00000386924.1:n.1152-226G=
NM_001024688.2:c.1152-226G=	NP_001019859.1:n.1152-226G=
NM_002485.4:c.1398-226G= , LRG_158t1:c.1398-226G=	NP_002476.2:n.1398-226G=
XM_011517044.1:c.1374-226G=	XP_011515346.1:n.1374-226G=
XM_011517045.1:c.1152-226G=	XP_011515347.1:n.1152-226G=
XM_011517046.1:c.1396-223G=	XP_011515348.1:n.1396-223G=
XR_928335.1:n.1534-223G=
XM_017013460.1:c.519-226G=	XP_016868949.1:n.519-226G=
XM_017013462.2:c.519-226G=	XP_016868951.1:n.519-226G=
XM_024447163.1:c.1152-226G=	XP_024302931.1:n.1152-226G=
XM_024447164.1:c.1152-226G=	XP_024302932.1:n.1152-226G=
XM_024447165.1:c.519-226G=	XP_024302933.1:n.519-226G=
NM_002485.5:c.1398-226G= MANE Select	NP_002476.2:n.1398-226G=
NM_001024688.3:c.1152-226G=	NP_001019859.1:n.1152-226G=