Canonical Allele Identifier: CA371655648

Gene: NBN

Linked Data

• MyVariant Identifiers: chr8:g.90965783C>A (hg19) ; chr8:g.89953555C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.89953555C>A , CM000670.2:g.89953555C>A	GRCh38
NC_000008.10:g.90965783C>A , CM000670.1:g.90965783C>A	GRCh37
NC_000008.9:g.91034959C>A	NCBI36
NG_008860.1:g.36117G>T , LRG_158:g.36117G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000494804.2:n.2836G>T
ENST00000517337.2:c.1288G>T	ENSP00000429971.2:p.Glu430Ter
ENST00000523444.2:c.1288G>T	ENSP00000428252.2:p.Glu430Ter
ENST00000697292.1:c.1534G>T	ENSP00000513229.1:p.Glu512Ter
ENST00000697293.1:c.1534G>T	ENSP00000513230.1:p.Glu512Ter
ENST00000697294.1:c.*1145G>T	ENSP00000513231.1:n.*1145G>T
ENST00000697295.1:c.*843G>T	ENSP00000513232.1:n.*843G>T
ENST00000697296.1:c.*1202G>T	ENSP00000513233.1:n.*1202G>T
ENST00000697297.1:n.3319G>T
ENST00000697298.1:c.1288G>T	ENSP00000513234.1:p.Glu430Ter
ENST00000697299.1:c.1288G>T	ENSP00000513235.1:p.Glu430Ter
ENST00000697300.1:c.*1138G>T	ENSP00000513236.1:n.*1138G>T
ENST00000697301.1:c.*1055G>T	ENSP00000513237.1:n.*1055G>T
ENST00000697302.1:c.*1055G>T	ENSP00000513238.1:n.*1055G>T
ENST00000697303.1:c.*1138G>T	ENSP00000513239.1:n.*1138G>T
ENST00000697304.1:c.1222G>T	ENSP00000513240.1:p.Glu408Ter
ENST00000697306.1:c.*534G>T	ENSP00000513241.1:n.*534G>T
ENST00000697307.1:c.1534G>T	ENSP00000513242.1:p.Glu512Ter
ENST00000697308.1:c.1534G>T	ENSP00000513243.1:p.Glu512Ter
ENST00000697309.1:c.1534G>T	ENSP00000513244.1:p.Glu512Ter
ENST00000697310.1:c.1534G>T	ENSP00000513245.1:p.Glu512Ter
ENST00000697311.1:c.1534G>T	ENSP00000513246.1:p.Glu512Ter
ENST00000697312.1:c.*932G>T	ENSP00000513247.1:n.*932G>T
ENST00000697313.1:n.2687+16809G>T
ENST00000697314.1:n.3325G>T
ENST00000697315.1:c.1534G>T	ENSP00000513248.1:p.Glu512Ter
ENST00000697316.1:n.1655G>T
ENST00000697317.1:n.1644G>T
ENST00000697318.1:n.1646G>T
ENST00000265433.8:c.1534G>T MANE Select	ENSP00000265433.4:p.Glu512Ter
ENST00000265433.7:c.1534G>T	ENSP00000265433.3:p.Glu512Ter
ENST00000396252.6:c.*1407G>T	ENSP00000379551.2:n.*1407G>T
ENST00000409330.5:c.1288G>T	ENSP00000386924.1:p.Glu430Ter
NM_001024688.2:c.1288G>T	NP_001019859.1:p.Glu430Ter
NM_002485.4:c.1534G>T , LRG_158t1:c.1534G>T	NP_002476.2:p.Glu512Ter
XM_011517044.1:c.1510G>T	XP_011515346.1:p.Glu504Ter
XM_011517045.1:c.1288G>T	XP_011515347.1:p.Glu430Ter
XR_928335.1:n.1673G>T
XM_017013460.1:c.655G>T	XP_016868949.1:p.Glu219Ter
XM_017013462.2:c.655G>T	XP_016868951.1:p.Glu219Ter
XM_024447163.1:c.1288G>T	XP_024302931.1:p.Glu430Ter
XM_024447164.1:c.1288G>T	XP_024302932.1:p.Glu430Ter
XM_024447165.1:c.655G>T	XP_024302933.1:p.Glu219Ter
NM_002485.5:c.1534G>T MANE Select	NP_002476.2:p.Glu512Ter
NM_001024688.3:c.1288G>T	NP_001019859.1:p.Glu430Ter