Canonical Allele Identifier: CA2687856744

Gene: NBN

Linked Data

• gnomAD v4: 8-89978097-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.89978098del , CM000670.2:g.89978098del	GRCh38
NC_000008.10:g.90990326del , CM000670.1:g.90990326del	GRCh37
NC_000008.9:g.91059502del	NCBI36
NG_008860.1:g.11574del , LRG_158:g.11574del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000494804.2:n.1886+122del
ENST00000517337.2:c.338+122del	ENSP00000429971.2:n.338+122del
ENST00000523444.2:c.338+122del	ENSP00000428252.2:n.338+122del
ENST00000697292.1:c.584+122del	ENSP00000513229.1:n.584+122del
ENST00000697293.1:c.584+122del	ENSP00000513230.1:n.584+122del
ENST00000697294.1:c.*195+122del	ENSP00000513231.1:n.*195+122del
ENST00000697295.1:c.37+6427del	ENSP00000513232.1:n.37+6427del
ENST00000697296.1:c.*252+122del	ENSP00000513233.1:n.*252+122del
ENST00000697297.1:n.2369+122del
ENST00000697298.1:c.338+122del	ENSP00000513234.1:n.338+122del
ENST00000697299.1:c.338+122del	ENSP00000513235.1:n.338+122del
ENST00000697300.1:c.*188+122del	ENSP00000513236.1:n.*188+122del
ENST00000697301.1:c.*105+122del	ENSP00000513237.1:n.*105+122del
ENST00000697302.1:c.*105+122del	ENSP00000513238.1:n.*105+122del
ENST00000697303.1:c.*188+122del	ENSP00000513239.1:n.*188+122del
ENST00000697304.1:c.584+122del	ENSP00000513240.1:n.584+122del
ENST00000697306.1:c.480+2636del	ENSP00000513241.1:n.480+2636del
ENST00000697307.1:c.584+122del	ENSP00000513242.1:n.584+122del
ENST00000697308.1:c.584+122del	ENSP00000513243.1:n.584+122del
ENST00000697309.1:c.584+122del	ENSP00000513244.1:n.584+122del
ENST00000697310.1:c.584+122del	ENSP00000513245.1:n.584+122del
ENST00000697311.1:c.584+122del	ENSP00000513246.1:n.584+122del
ENST00000697312.1:c.480+2636del	ENSP00000513247.1:n.480+2636del
ENST00000697313.1:n.2375+122del
ENST00000697314.1:n.2375+122del
ENST00000697315.1:c.584+122del	ENSP00000513248.1:n.584+122del
ENST00000697316.1:n.705+122del
ENST00000697317.1:n.694+122del
ENST00000697318.1:n.696+122del
ENST00000265433.8:c.584+122del MANE Select	ENSP00000265433.4:n.584+122del
ENST00000265433.7:c.584+122del	ENSP00000265433.3:n.584+122del
ENST00000396252.6:c.*457+122del	ENSP00000379551.2:n.*457+122del
ENST00000409330.5:c.338+122del	ENSP00000386924.1:n.338+122del
ENST00000517772.5:c.338+122del	ENSP00000428717.1:n.338+122del
ENST00000519426.5:c.320+3277del	ENSP00000430983.1:n.320+3277del
NM_001024688.2:c.338+122del	NP_001019859.1:n.338+122del
NM_002485.4:c.584+122del , LRG_158t1:c.584+122del	NP_002476.2:n.584+122del
XM_011517044.1:c.560+122del	XP_011515346.1:n.560+122del
XM_011517045.1:c.338+122del	XP_011515347.1:n.338+122del
XM_011517046.1:c.584+122del	XP_011515348.1:n.584+122del
XR_928335.1:n.721+122del
XM_017013460.1:c.-296+122del	XP_016868949.1:n.-296+122del
XM_017013462.2:c.-296+2636del	XP_016868951.1:n.-296+2636del
XM_024447163.1:c.338+122del	XP_024302931.1:n.338+122del
XM_024447164.1:c.338+122del	XP_024302932.1:n.338+122del
XM_024447165.1:c.-296+122del	XP_024302933.1:n.-296+122del
NM_002485.5:c.584+122del MANE Select	NP_002476.2:n.584+122del
NM_001024688.3:c.338+122del	NP_001019859.1:n.338+122del