Canonical Allele Identifier: CA1801415407
Gene: NBN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.89937043A= , CM000670.2:g.89937043A= GRCh38
NC_000008.10:g.90949271A= , CM000670.1:g.90949271A= GRCh37
NC_000008.9:g.91018447A= NCBI36
NG_008860.1:g.52629T= , LRG_158:g.52629T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000474821.2:n.3637T=
ENST00000494804.2:n.3519T=
ENST00000517337.2:c.1971T= ENSP00000429971.2:p.Leu657=
ENST00000523444.2:c.1971T= ENSP00000428252.2:p.Leu657=
ENST00000697292.1:c.2217T= ENSP00000513229.1:p.Leu739=
ENST00000697293.1:c.2268T= ENSP00000513230.1:p.Leu756=
ENST00000697294.1:c.*1828T= ENSP00000513231.1:n.*1828T=
ENST00000697295.1:c.*1526T= ENSP00000513232.1:n.*1526T=
ENST00000697296.1:c.*1885T= ENSP00000513233.1:n.*1885T=
ENST00000697297.1:n.4002T=
ENST00000697298.1:c.1971T= ENSP00000513234.1:p.Leu657=
ENST00000697299.1:c.1971T= ENSP00000513235.1:p.Leu657=
ENST00000697300.1:c.*1821T= ENSP00000513236.1:n.*1821T=
ENST00000697301.1:c.*1738T= ENSP00000513237.1:n.*1738T=
ENST00000697302.1:c.*1738T= ENSP00000513238.1:n.*1738T=
ENST00000697303.1:c.*1821T= ENSP00000513239.1:n.*1821T=
ENST00000697304.1:c.1905T= ENSP00000513240.1:p.Leu635=
ENST00000697305.1:n.2484T=
ENST00000697306.1:c.*2768T= ENSP00000513241.1:n.*2768T=
ENST00000697307.1:c.1992T= ENSP00000513242.1:p.Leu664=
ENST00000697308.1:c.2148T= ENSP00000513243.1:p.Leu716=
ENST00000697309.1:c.2185-1431T= ENSP00000513244.1:n.2185-1431T=
ENST00000697310.1:c.2217T= ENSP00000513245.1:p.Leu739=
ENST00000697311.1:c.*482T= ENSP00000513246.1:n.*482T=
ENST00000697312.1:c.*1670T= ENSP00000513247.1:n.*1670T=
ENST00000697313.1:n.2688-1431T=
ENST00000697314.1:n.3637-1431T=
ENST00000697315.1:c.*121T= ENSP00000513248.1:n.*121T=
ENST00000697316.1:n.2338T=
ENST00000265433.8:c.2217T= MANE Select ENSP00000265433.4:p.Leu739=
ENST00000265433.7:c.2217T= ENSP00000265433.3:p.Leu739=
ENST00000396252.6:c.*2090T= ENSP00000379551.2:n.*2090T=
ENST00000409330.5:c.1971T= ENSP00000386924.1:p.Leu657=
ENST00000474821.1:n.305T=
ENST00000613033.1:c.327T= ENSP00000484487.1:p.Leu109=
NM_001024688.2:c.1971T= NP_001019859.1:p.Leu657=
NM_002485.4:c.2217T= , LRG_158t1:c.2217T= NP_002476.2:p.Leu739=
XM_011517044.1:c.2193T= XP_011515346.1:p.Leu731=
XM_011517045.1:c.1971T= XP_011515347.1:p.Leu657=
XM_017013460.1:c.1338T= XP_016868949.1:p.Leu446=
XM_017013462.2:c.1338T= XP_016868951.1:p.Leu446=
XM_024447163.1:c.1971T= XP_024302931.1:p.Leu657=
XM_024447164.1:c.1971T= XP_024302932.1:p.Leu657=
XM_024447165.1:c.1338T= XP_024302933.1:p.Leu446=
NM_002485.5:c.2217T= MANE Select NP_002476.2:p.Leu739=
NM_001024688.3:c.1971T= NP_001019859.1:p.Leu657=