Canonical Allele Identifier: CA1801471071
Gene: NBN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.89984534G= , CM000670.2:g.89984534G= GRCh38
NC_000008.10:g.90996762G= , CM000670.1:g.90996762G= GRCh37
NC_000008.9:g.91065938G= NCBI36
NG_008860.1:g.5138C= , LRG_158:g.5138C=

Transcript Alleles

HGVS Amino-acid change
ENST00000494804.2:n.132C=
ENST00000523444.2:c.-269C= ENSP00000428252.2:n.-269C=
ENST00000697292.1:c.28C= ENSP00000513229.1:p.Pro10=
ENST00000697293.1:c.28C= ENSP00000513230.1:p.Pro10=
ENST00000697294.1:c.28C= ENSP00000513231.1:p.Pro10=
ENST00000697295.1:c.28C= ENSP00000513232.1:p.Pro10=
ENST00000697296.1:c.28C= ENSP00000513233.1:p.Pro10=
ENST00000697297.1:n.134C=
ENST00000697298.1:c.-452C= ENSP00000513234.1:n.-452C=
ENST00000697299.1:c.-85C= ENSP00000513235.1:n.-85C=
ENST00000697300.1:c.-269C= ENSP00000513236.1:n.-269C=
ENST00000697301.1:c.-269C= ENSP00000513237.1:n.-269C=
ENST00000697302.1:c.28C= ENSP00000513238.1:p.Pro10=
ENST00000697303.1:c.28C= ENSP00000513239.1:p.Pro10=
ENST00000697304.1:c.28C= ENSP00000513240.1:p.Pro10=
ENST00000697306.1:c.28C= ENSP00000513241.1:p.Pro10=
ENST00000697307.1:c.28C= ENSP00000513242.1:p.Pro10=
ENST00000697308.1:c.28C= ENSP00000513243.1:p.Pro10=
ENST00000697309.1:c.28C= ENSP00000513244.1:p.Pro10=
ENST00000697310.1:c.28C= ENSP00000513245.1:p.Pro10=
ENST00000697311.1:c.28C= ENSP00000513246.1:p.Pro10=
ENST00000697312.1:c.28C= ENSP00000513247.1:p.Pro10=
ENST00000697313.1:n.140C=
ENST00000697314.1:n.140C=
ENST00000697315.1:c.28C= ENSP00000513248.1:p.Pro10=
ENST00000697316.1:n.149C=
ENST00000697317.1:n.138C=
ENST00000697318.1:n.140C=
ENST00000265433.8:c.28C= MANE Select ENSP00000265433.4:p.Pro10=
ENST00000265433.7:c.28C= ENSP00000265433.3:p.Pro10=
ENST00000396252.6:c.28C= ENSP00000379551.2:p.Pro10=
ENST00000494804.1:n.132C=
ENST00000519426.5:c.28C= ENSP00000430983.1:p.Pro10=
ENST00000523444.1:c.28C= ENSP00000428252.1:p.Pro10=
NM_001024688.2:c.-269C= NP_001019859.1:n.-269C=
NM_002485.4:c.28C= , LRG_158t1:c.28C= NP_002476.2:p.Pro10=
XM_011517046.1:c.28C= XP_011515348.1:p.Pro10=
XR_928335.1:n.165C=
XM_017013460.1:c.-992C= XP_016868949.1:n.-992C=
XM_017013462.2:c.-798C= XP_016868951.1:n.-798C=
XM_024447165.1:c.-942C= XP_024302933.1:n.-942C=
NM_002485.5:c.28C= MANE Select NP_002476.2:p.Pro10=
NM_001024688.3:c.-269C= NP_001019859.1:n.-269C=