Canonical Allele Identifier: CA1801415338

Gene: NBN

Linked Data

• dbSNP Id: rs1809710691

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.89936893del , CM000670.2:g.89936893del	GRCh38
NC_000008.10:g.90949121del , CM000670.1:g.90949121del	GRCh37
NC_000008.9:g.91018297del	NCBI36
NG_008860.1:g.52783del , LRG_158:g.52783del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474821.2:n.3654+137del
ENST00000494804.2:n.3536+137del
ENST00000517337.2:c.1988+137del	ENSP00000429971.2:n.1988+137del
ENST00000523444.2:c.1988+137del	ENSP00000428252.2:n.1988+137del
ENST00000697292.1:c.2234+137del	ENSP00000513229.1:n.2234+137del
ENST00000697293.1:c.2285+137del	ENSP00000513230.1:n.2285+137del
ENST00000697294.1:c.*1845+137del	ENSP00000513231.1:n.*1845+137del
ENST00000697295.1:c.*1543+137del	ENSP00000513232.1:n.*1543+137del
ENST00000697296.1:c.*1902+137del	ENSP00000513233.1:n.*1902+137del
ENST00000697297.1:n.4019+137del
ENST00000697298.1:c.1988+137del	ENSP00000513234.1:n.1988+137del
ENST00000697299.1:c.1988+137del	ENSP00000513235.1:n.1988+137del
ENST00000697300.1:c.*1838+137del	ENSP00000513236.1:n.*1838+137del
ENST00000697301.1:c.*1755+137del	ENSP00000513237.1:n.*1755+137del
ENST00000697302.1:c.*1755+137del	ENSP00000513238.1:n.*1755+137del
ENST00000697303.1:c.*1838+137del	ENSP00000513239.1:n.*1838+137del
ENST00000697304.1:c.1922+137del	ENSP00000513240.1:n.1922+137del
ENST00000697305.1:n.2501+137del
ENST00000697306.1:c.*2785+137del	ENSP00000513241.1:n.*2785+137del
ENST00000697307.1:c.2009+137del	ENSP00000513242.1:n.2009+137del
ENST00000697308.1:c.2165+137del	ENSP00000513243.1:n.2165+137del
ENST00000697309.1:c.2185-1277del	ENSP00000513244.1:n.2185-1277del
ENST00000697310.1:c.2234+137del	ENSP00000513245.1:n.2234+137del
ENST00000697311.1:c.*499+137del	ENSP00000513246.1:n.*499+137del
ENST00000697312.1:c.*1687+137del	ENSP00000513247.1:n.*1687+137del
ENST00000697313.1:n.2688-1277del
ENST00000697314.1:n.3637-1277del
ENST00000697315.1:c.*138+137del	ENSP00000513248.1:n.*138+137del
ENST00000697316.1:n.2492del
ENST00000265433.8:c.2234+137del MANE Select	ENSP00000265433.4:n.2234+137del
ENST00000265433.7:c.2234+137del	ENSP00000265433.3:n.2234+137del
ENST00000396252.6:c.*2107+137del	ENSP00000379551.2:n.*2107+137del
ENST00000409330.5:c.1988+137del	ENSP00000386924.1:n.1988+137del
ENST00000474821.1:n.322+137del
ENST00000613033.1:c.344+137del	ENSP00000484487.1:n.344+137del
NM_001024688.2:c.1988+137del	NP_001019859.1:n.1988+137del
NM_002485.4:c.2234+137del , LRG_158t1:c.2234+137del	NP_002476.2:n.2234+137del
XM_011517044.1:c.2210+137del	XP_011515346.1:n.2210+137del
XM_011517045.1:c.1988+137del	XP_011515347.1:n.1988+137del
XM_017013460.1:c.1355+137del	XP_016868949.1:n.1355+137del
XM_017013462.2:c.1355+137del	XP_016868951.1:n.1355+137del
XM_024447163.1:c.1988+137del	XP_024302931.1:n.1988+137del
XM_024447164.1:c.1988+137del	XP_024302932.1:n.1988+137del
XM_024447165.1:c.1355+137del	XP_024302933.1:n.1355+137del
NM_002485.5:c.2234+137del MANE Select	NP_002476.2:n.2234+137del
NM_001024688.3:c.1988+137del	NP_001019859.1:n.1988+137del