Canonical Allele Identifier: CA371674744

Gene: NBN

Linked Data

• MyVariant Identifiers: chr8:g.90949257A>G (hg19) ; chr8:g.89937029A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.89937029A>G , CM000670.2:g.89937029A>G	GRCh38
NC_000008.10:g.90949257A>G , CM000670.1:g.90949257A>G	GRCh37
NC_000008.9:g.91018433A>G	NCBI36
NG_008860.1:g.52643T>C , LRG_158:g.52643T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474821.2:n.3651T>C
ENST00000494804.2:n.3533T>C
ENST00000517337.2:c.1985T>C	ENSP00000429971.2:p.Phe662Ser
ENST00000523444.2:c.1985T>C	ENSP00000428252.2:p.Phe662Ser
ENST00000697292.1:c.2231T>C	ENSP00000513229.1:p.Phe744Ser
ENST00000697293.1:c.2282T>C	ENSP00000513230.1:p.Phe761Ser
ENST00000697294.1:c.*1842T>C	ENSP00000513231.1:n.*1842T>C
ENST00000697295.1:c.*1540T>C	ENSP00000513232.1:n.*1540T>C
ENST00000697296.1:c.*1899T>C	ENSP00000513233.1:n.*1899T>C
ENST00000697297.1:n.4016T>C
ENST00000697298.1:c.1985T>C	ENSP00000513234.1:p.Phe662Ser
ENST00000697299.1:c.1985T>C	ENSP00000513235.1:p.Phe662Ser
ENST00000697300.1:c.*1835T>C	ENSP00000513236.1:n.*1835T>C
ENST00000697301.1:c.*1752T>C	ENSP00000513237.1:n.*1752T>C
ENST00000697302.1:c.*1752T>C	ENSP00000513238.1:n.*1752T>C
ENST00000697303.1:c.*1835T>C	ENSP00000513239.1:n.*1835T>C
ENST00000697304.1:c.1919T>C	ENSP00000513240.1:p.Phe640Ser
ENST00000697305.1:n.2498T>C
ENST00000697306.1:c.*2782T>C	ENSP00000513241.1:n.*2782T>C
ENST00000697307.1:c.2006T>C	ENSP00000513242.1:p.Phe669Ser
ENST00000697308.1:c.2162T>C	ENSP00000513243.1:p.Phe721Ser
ENST00000697309.1:c.2185-1417T>C	ENSP00000513244.1:n.2185-1417T>C
ENST00000697310.1:c.2231T>C	ENSP00000513245.1:p.Phe744Ser
ENST00000697311.1:c.*496T>C	ENSP00000513246.1:n.*496T>C
ENST00000697312.1:c.*1684T>C	ENSP00000513247.1:n.*1684T>C
ENST00000697313.1:n.2688-1417T>C
ENST00000697314.1:n.3637-1417T>C
ENST00000697315.1:c.*135T>C	ENSP00000513248.1:n.*135T>C
ENST00000697316.1:n.2352T>C
ENST00000265433.8:c.2231T>C MANE Select	ENSP00000265433.4:p.Phe744Ser
ENST00000265433.7:c.2231T>C	ENSP00000265433.3:p.Phe744Ser
ENST00000396252.6:c.*2104T>C	ENSP00000379551.2:n.*2104T>C
ENST00000409330.5:c.1985T>C	ENSP00000386924.1:p.Phe662Ser
ENST00000474821.1:n.319T>C
ENST00000613033.1:c.341T>C	ENSP00000484487.1:p.Phe114Ser
NM_001024688.2:c.1985T>C	NP_001019859.1:p.Phe662Ser
NM_002485.4:c.2231T>C , LRG_158t1:c.2231T>C	NP_002476.2:p.Phe744Ser
XM_011517044.1:c.2207T>C	XP_011515346.1:p.Phe736Ser
XM_011517045.1:c.1985T>C	XP_011515347.1:p.Phe662Ser
XM_017013460.1:c.1352T>C	XP_016868949.1:p.Phe451Ser
XM_017013462.2:c.1352T>C	XP_016868951.1:p.Phe451Ser
XM_024447163.1:c.1985T>C	XP_024302931.1:p.Phe662Ser
XM_024447164.1:c.1985T>C	XP_024302932.1:p.Phe662Ser
XM_024447165.1:c.1352T>C	XP_024302933.1:p.Phe451Ser
NM_002485.5:c.2231T>C MANE Select	NP_002476.2:p.Phe744Ser
NM_001024688.3:c.1985T>C	NP_001019859.1:p.Phe662Ser