Canonical Allele Identifier: CA1801422924

Gene: NBN

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.89953538G= , CM000670.2:g.89953538G=	GRCh38
NC_000008.10:g.90965766G= , CM000670.1:g.90965766G=	GRCh37
NC_000008.9:g.91034942G=	NCBI36
NG_008860.1:g.36134C= , LRG_158:g.36134C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000494804.2:n.2853C=
ENST00000517337.2:c.1305C=	ENSP00000429971.2:p.Asn435=
ENST00000523444.2:c.1305C=	ENSP00000428252.2:p.Asn435=
ENST00000697292.1:c.1551C=	ENSP00000513229.1:p.Asn517=
ENST00000697293.1:c.1551C=	ENSP00000513230.1:p.Asn517=
ENST00000697294.1:c.*1162C=	ENSP00000513231.1:n.*1162C=
ENST00000697295.1:c.*860C=	ENSP00000513232.1:n.*860C=
ENST00000697296.1:c.*1219C=	ENSP00000513233.1:n.*1219C=
ENST00000697297.1:n.3336C=
ENST00000697298.1:c.1305C=	ENSP00000513234.1:p.Asn435=
ENST00000697299.1:c.1305C=	ENSP00000513235.1:p.Asn435=
ENST00000697300.1:c.*1155C=	ENSP00000513236.1:n.*1155C=
ENST00000697301.1:c.*1072C=	ENSP00000513237.1:n.*1072C=
ENST00000697302.1:c.*1072C=	ENSP00000513238.1:n.*1072C=
ENST00000697303.1:c.*1155C=	ENSP00000513239.1:n.*1155C=
ENST00000697304.1:c.1239C=	ENSP00000513240.1:p.Asn413=
ENST00000697306.1:c.*551C=	ENSP00000513241.1:n.*551C=
ENST00000697307.1:c.1551C=	ENSP00000513242.1:p.Asn517=
ENST00000697308.1:c.1551C=	ENSP00000513243.1:p.Asn517=
ENST00000697309.1:c.1551C=	ENSP00000513244.1:p.Asn517=
ENST00000697310.1:c.1551C=	ENSP00000513245.1:p.Asn517=
ENST00000697311.1:c.1551C=	ENSP00000513246.1:p.Asn517=
ENST00000697312.1:c.*949C=	ENSP00000513247.1:n.*949C=
ENST00000697313.1:n.2687+16826C=
ENST00000697314.1:n.3342C=
ENST00000697315.1:c.1551C=	ENSP00000513248.1:p.Asn517=
ENST00000697316.1:n.1672C=
ENST00000697317.1:n.1661C=
ENST00000697318.1:n.1663C=
ENST00000265433.8:c.1551C= MANE Select	ENSP00000265433.4:p.Asn517=
ENST00000265433.7:c.1551C=	ENSP00000265433.3:p.Asn517=
ENST00000396252.6:c.*1424C=	ENSP00000379551.2:n.*1424C=
ENST00000409330.5:c.1305C=	ENSP00000386924.1:p.Asn435=
NM_001024688.2:c.1305C=	NP_001019859.1:p.Asn435=
NM_002485.4:c.1551C= , LRG_158t1:c.1551C=	NP_002476.2:p.Asn517=
XM_011517044.1:c.1527C=	XP_011515346.1:p.Asn509=
XM_011517045.1:c.1305C=	XP_011515347.1:p.Asn435=
XR_928335.1:n.1690C=
XM_017013460.1:c.672C=	XP_016868949.1:p.Asn224=
XM_017013462.2:c.672C=	XP_016868951.1:p.Asn224=
XM_024447163.1:c.1305C=	XP_024302931.1:p.Asn435=
XM_024447164.1:c.1305C=	XP_024302932.1:p.Asn435=
XM_024447165.1:c.672C=	XP_024302933.1:p.Asn224=
NM_002485.5:c.1551C= MANE Select	NP_002476.2:p.Asn517=
NM_001024688.3:c.1305C=	NP_001019859.1:p.Asn435=