Canonical Allele Identifier: CA371675407

Gene: NBN

Linked Data

• MyVariant Identifiers: chr8:g.90955513C>G (hg19) ; chr8:g.89943285C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.89943285C>G , CM000670.2:g.89943285C>G	GRCh38
NC_000008.10:g.90955513C>G , CM000670.1:g.90955513C>G	GRCh37
NC_000008.9:g.91024689C>G	NCBI36
NG_008860.1:g.46387G>C , LRG_158:g.46387G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000494804.2:n.3454G>C
ENST00000517337.2:c.1906G>C	ENSP00000429971.2:p.Glu636Gln
ENST00000523444.2:c.1906G>C	ENSP00000428252.2:p.Glu636Gln
ENST00000697292.1:c.2152G>C	ENSP00000513229.1:p.Glu718Gln
ENST00000697293.1:c.2152G>C	ENSP00000513230.1:p.Glu718Gln
ENST00000697294.1:c.*1763G>C	ENSP00000513231.1:n.*1763G>C
ENST00000697295.1:c.*1461G>C	ENSP00000513232.1:n.*1461G>C
ENST00000697296.1:c.*1820G>C	ENSP00000513233.1:n.*1820G>C
ENST00000697297.1:n.3937G>C
ENST00000697298.1:c.1906G>C	ENSP00000513234.1:p.Glu636Gln
ENST00000697299.1:c.1906G>C	ENSP00000513235.1:p.Glu636Gln
ENST00000697300.1:c.*1756G>C	ENSP00000513236.1:n.*1756G>C
ENST00000697301.1:c.*1673G>C	ENSP00000513237.1:n.*1673G>C
ENST00000697302.1:c.*1673G>C	ENSP00000513238.1:n.*1673G>C
ENST00000697303.1:c.*1756G>C	ENSP00000513239.1:n.*1756G>C
ENST00000697304.1:c.1840G>C	ENSP00000513240.1:p.Glu614Gln
ENST00000697305.1:n.2419G>C
ENST00000697306.1:c.*2703G>C	ENSP00000513241.1:n.*2703G>C
ENST00000697307.1:c.1927G>C	ENSP00000513242.1:p.Glu643Gln
ENST00000697308.1:c.2083G>C	ENSP00000513243.1:p.Glu695Gln
ENST00000697309.1:c.2152G>C	ENSP00000513244.1:p.Glu718Gln
ENST00000697310.1:c.2152G>C	ENSP00000513245.1:p.Glu718Gln
ENST00000697311.1:c.2152G>C	ENSP00000513246.1:p.Glu718Gln
ENST00000697312.1:c.*1550G>C	ENSP00000513247.1:n.*1550G>C
ENST00000697313.1:n.2688-7673G>C
ENST00000697314.1:n.3637-7673G>C
ENST00000697315.1:c.2152G>C	ENSP00000513248.1:p.Glu718Gln
ENST00000697316.1:n.2273G>C
ENST00000265433.8:c.2152G>C MANE Select	ENSP00000265433.4:p.Glu718Gln
ENST00000265433.7:c.2152G>C	ENSP00000265433.3:p.Glu718Gln
ENST00000396252.6:c.*2025G>C	ENSP00000379551.2:n.*2025G>C
ENST00000409330.5:c.1906G>C	ENSP00000386924.1:p.Glu636Gln
ENST00000613033.1:c.262G>C	ENSP00000484487.1:p.Glu88Gln
NM_001024688.2:c.1906G>C	NP_001019859.1:p.Glu636Gln
NM_002485.4:c.2152G>C , LRG_158t1:c.2152G>C	NP_002476.2:p.Glu718Gln
XM_011517044.1:c.2128G>C	XP_011515346.1:p.Glu710Gln
XM_011517045.1:c.1906G>C	XP_011515347.1:p.Glu636Gln
XM_017013460.1:c.1273G>C	XP_016868949.1:p.Glu425Gln
XM_017013462.2:c.1273G>C	XP_016868951.1:p.Glu425Gln
XM_024447163.1:c.1906G>C	XP_024302931.1:p.Glu636Gln
XM_024447164.1:c.1906G>C	XP_024302932.1:p.Glu636Gln
XM_024447165.1:c.1273G>C	XP_024302933.1:p.Glu425Gln
NM_002485.5:c.2152G>C MANE Select	NP_002476.2:p.Glu718Gln
NM_001024688.3:c.1906G>C	NP_001019859.1:p.Glu636Gln