Canonical Allele Identifier: CA2695209954

Gene: NBN

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.89984525del , CM000670.2:g.89984525del	GRCh38
NC_000008.10:g.90996753del , CM000670.1:g.90996753del	GRCh37
NC_000008.9:g.91065929del	NCBI36
NG_008860.1:g.5148del , LRG_158:g.5148del

Transcript Alleles

HGVS	Amino-acid change
ENST00000494804.2:n.141+1del
ENST00000523444.2:c.-260+1del
ENST00000697292.1:c.37+1del
ENST00000697293.1:c.37+1del
ENST00000697294.1:c.37+1del
ENST00000697295.1:c.37+1del
ENST00000697296.1:c.37+1del
ENST00000697297.1:n.143+1del
ENST00000697298.1:c.-443+1del
ENST00000697299.1:c.-76+1del
ENST00000697300.1:c.-260+1del
ENST00000697301.1:c.-260+1del
ENST00000697302.1:c.37+1del
ENST00000697303.1:c.37+1del
ENST00000697304.1:c.37+1del
ENST00000697306.1:c.37+1del
ENST00000697307.1:c.37+1del
ENST00000697308.1:c.37+1del
ENST00000697309.1:c.37+1del
ENST00000697310.1:c.37+1del
ENST00000697311.1:c.37+1del
ENST00000697312.1:c.37+1del
ENST00000697313.1:n.149+1del
ENST00000697314.1:n.149+1del
ENST00000697315.1:c.37+1del
ENST00000697316.1:n.158+1del
ENST00000697317.1:n.147+1del
ENST00000697318.1:n.149+1del
ENST00000265433.8:c.37+1del
ENST00000265433.7:c.37+1del
ENST00000396252.6:c.37+1del
ENST00000494804.1:n.141+1del
ENST00000519426.5:c.37+1del
ENST00000523444.1:c.37+1del
NM_001024688.2:c.-260+1del
NM_002485.4:c.37+1del , LRG_158t1:c.37+1del
XM_011517046.1:c.37+1del
XR_928335.1:n.174+1del
XM_017013460.1:c.-983+1del
XM_017013462.2:c.-789+1del
XM_024447165.1:c.-933+1del
NM_002485.5:c.37+1del
NM_001024688.3:c.-260+1del