Canonical Allele Identifier: CA181268861

Gene: NBN

Linked Data

• dbSNP Id: rs984816682
• gnomAD v2: 8-90949413-TCAC-T
• gnomAD v3: 8-89937185-TCAC-T
• gnomAD v4: 8-89937185-TCAC-T
• MyVariant Identifiers: chr8:g.90949414_90949416del (hg19) ; chr8:g.89937186_89937188del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.89937189_89937191del , CM000670.2:g.89937189_89937191del	GRCh38
NC_000008.10:g.90949417_90949419del , CM000670.1:g.90949417_90949419del	GRCh37
NC_000008.9:g.91018593_91018595del	NCBI36
NG_008860.1:g.52484_52486del , LRG_158:g.52484_52486del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474821.2:n.3492_3494del
ENST00000494804.2:n.3487-113_3487-111del
ENST00000517337.2:c.1939-113_1939-111del	ENSP00000429971.2:n.1939-113_1939-111del
ENST00000523444.2:c.1939-113_1939-111del	ENSP00000428252.2:n.1939-113_1939-111del
ENST00000697292.1:c.2185-113_2185-111del	ENSP00000513229.1:n.2185-113_2185-111del
ENST00000697293.1:c.2236-113_2236-111del	ENSP00000513230.1:n.2236-113_2236-111del
ENST00000697294.1:c.*1796-113_*1796-111del	ENSP00000513231.1:n.*1796-113_*1796-111del
ENST00000697295.1:c.*1494-113_*1494-111del	ENSP00000513232.1:n.*1494-113_*1494-111del
ENST00000697296.1:c.*1853-113_*1853-111del	ENSP00000513233.1:n.*1853-113_*1853-111del
ENST00000697297.1:n.3970-113_3970-111del
ENST00000697298.1:c.1939-113_1939-111del	ENSP00000513234.1:n.1939-113_1939-111del
ENST00000697299.1:c.1939-113_1939-111del	ENSP00000513235.1:n.1939-113_1939-111del
ENST00000697300.1:c.*1789-113_*1789-111del	ENSP00000513236.1:n.*1789-113_*1789-111del
ENST00000697301.1:c.*1706-113_*1706-111del	ENSP00000513237.1:n.*1706-113_*1706-111del
ENST00000697302.1:c.*1706-113_*1706-111del	ENSP00000513238.1:n.*1706-113_*1706-111del
ENST00000697303.1:c.*1789-113_*1789-111del	ENSP00000513239.1:n.*1789-113_*1789-111del
ENST00000697304.1:c.1873-113_1873-111del	ENSP00000513240.1:n.1873-113_1873-111del
ENST00000697305.1:n.2452-113_2452-111del
ENST00000697306.1:c.*2736-113_*2736-111del	ENSP00000513241.1:n.*2736-113_*2736-111del
ENST00000697307.1:c.1960-113_1960-111del	ENSP00000513242.1:n.1960-113_1960-111del
ENST00000697308.1:c.2116-113_2116-111del	ENSP00000513243.1:n.2116-113_2116-111del
ENST00000697309.1:c.2185-1576_2185-1574del	ENSP00000513244.1:n.2185-1576_2185-1574del
ENST00000697310.1:c.2185-113_2185-111del	ENSP00000513245.1:n.2185-113_2185-111del
ENST00000697311.1:c.*450-113_*450-111del	ENSP00000513246.1:n.*450-113_*450-111del
ENST00000697312.1:c.*1638-113_*1638-111del	ENSP00000513247.1:n.*1638-113_*1638-111del
ENST00000697313.1:n.2688-1576_2688-1574del
ENST00000697314.1:n.3637-1576_3637-1574del
ENST00000697315.1:c.*89-113_*89-111del	ENSP00000513248.1:n.*89-113_*89-111del
ENST00000697316.1:n.2306-113_2306-111del
ENST00000265433.8:c.2185-113_2185-111del MANE Select	ENSP00000265433.4:n.2185-113_2185-111del
ENST00000265433.7:c.2185-113_2185-111del	ENSP00000265433.3:n.2185-113_2185-111del
ENST00000396252.6:c.*2058-113_*2058-111del	ENSP00000379551.2:n.*2058-113_*2058-111del
ENST00000409330.5:c.1939-113_1939-111del	ENSP00000386924.1:n.1939-113_1939-111del
ENST00000474821.1:n.160_162del
ENST00000613033.1:c.295-113_295-111del	ENSP00000484487.1:n.295-113_295-111del
NM_001024688.2:c.1939-113_1939-111del	NP_001019859.1:n.1939-113_1939-111del
NM_002485.4:c.2185-113_2185-111del , LRG_158t1:c.2185-113_2185-111del	NP_002476.2:n.2185-113_2185-111del
XM_011517044.1:c.2161-113_2161-111del	XP_011515346.1:n.2161-113_2161-111del
XM_011517045.1:c.1939-113_1939-111del	XP_011515347.1:n.1939-113_1939-111del
XM_017013460.1:c.1306-113_1306-111del	XP_016868949.1:n.1306-113_1306-111del
XM_017013462.2:c.1306-113_1306-111del	XP_016868951.1:n.1306-113_1306-111del
XM_024447163.1:c.1939-113_1939-111del	XP_024302931.1:n.1939-113_1939-111del
XM_024447164.1:c.1939-113_1939-111del	XP_024302932.1:n.1939-113_1939-111del
XM_024447165.1:c.1306-113_1306-111del	XP_024302933.1:n.1306-113_1306-111del
NM_002485.5:c.2185-113_2185-111del MANE Select	NP_002476.2:n.2185-113_2185-111del
NM_001024688.3:c.1939-113_1939-111del	NP_001019859.1:n.1939-113_1939-111del