Canonical Allele Identifier: CA371676332

Gene: NBN

Linked Data

• MyVariant Identifiers: chr8:g.90958376A>G (hg19) ; chr8:g.89946148A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.89946148A>G , CM000670.2:g.89946148A>G	GRCh38
NC_000008.10:g.90958376A>G , CM000670.1:g.90958376A>G	GRCh37
NC_000008.9:g.91027552A>G	NCBI36
NG_008860.1:g.43524T>C , LRG_158:g.43524T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000494804.2:n.3364T>C
ENST00000517337.2:c.1816T>C	ENSP00000429971.2:p.Phe606Leu
ENST00000523444.2:c.1816T>C	ENSP00000428252.2:p.Phe606Leu
ENST00000697292.1:c.2062T>C	ENSP00000513229.1:p.Phe688Leu
ENST00000697293.1:c.2062T>C	ENSP00000513230.1:p.Phe688Leu
ENST00000697294.1:c.*1673T>C	ENSP00000513231.1:n.*1673T>C
ENST00000697295.1:c.*1371T>C	ENSP00000513232.1:n.*1371T>C
ENST00000697296.1:c.*1730T>C	ENSP00000513233.1:n.*1730T>C
ENST00000697297.1:n.3847T>C
ENST00000697298.1:c.1816T>C	ENSP00000513234.1:p.Phe606Leu
ENST00000697299.1:c.1816T>C	ENSP00000513235.1:p.Phe606Leu
ENST00000697300.1:c.*1666T>C	ENSP00000513236.1:n.*1666T>C
ENST00000697301.1:c.*1583T>C	ENSP00000513237.1:n.*1583T>C
ENST00000697302.1:c.*1583T>C	ENSP00000513238.1:n.*1583T>C
ENST00000697303.1:c.*1666T>C	ENSP00000513239.1:n.*1666T>C
ENST00000697304.1:c.1750T>C	ENSP00000513240.1:p.Phe584Leu
ENST00000697306.1:c.*2613T>C	ENSP00000513241.1:n.*2613T>C
ENST00000697307.1:c.1846-2782T>C	ENSP00000513242.1:n.1846-2782T>C
ENST00000697308.1:c.1993T>C	ENSP00000513243.1:p.Phe665Leu
ENST00000697309.1:c.2062T>C	ENSP00000513244.1:p.Phe688Leu
ENST00000697310.1:c.2062T>C	ENSP00000513245.1:p.Phe688Leu
ENST00000697311.1:c.2062T>C	ENSP00000513246.1:p.Phe688Leu
ENST00000697312.1:c.*1460T>C	ENSP00000513247.1:n.*1460T>C
ENST00000697313.1:n.2688-10536T>C
ENST00000697314.1:n.3636+7096T>C
ENST00000697315.1:c.2062T>C	ENSP00000513248.1:p.Phe688Leu
ENST00000697316.1:n.2183T>C
ENST00000697317.1:n.2153T>C
ENST00000265433.8:c.2062T>C MANE Select	ENSP00000265433.4:p.Phe688Leu
ENST00000265433.7:c.2062T>C	ENSP00000265433.3:p.Phe688Leu
ENST00000396252.6:c.*1935T>C	ENSP00000379551.2:n.*1935T>C
ENST00000409330.5:c.1816T>C	ENSP00000386924.1:p.Phe606Leu
ENST00000520325.1:n.478T>C
ENST00000613033.1:c.180+1676T>C	ENSP00000484487.1:n.180+1676T>C
NM_001024688.2:c.1816T>C	NP_001019859.1:p.Phe606Leu
NM_002485.4:c.2062T>C , LRG_158t1:c.2062T>C	NP_002476.2:p.Phe688Leu
XM_011517044.1:c.2038T>C	XP_011515346.1:p.Phe680Leu
XM_011517045.1:c.1816T>C	XP_011515347.1:p.Phe606Leu
XM_017013460.1:c.1183T>C	XP_016868949.1:p.Phe395Leu
XM_017013462.2:c.1183T>C	XP_016868951.1:p.Phe395Leu
XM_024447163.1:c.1816T>C	XP_024302931.1:p.Phe606Leu
XM_024447164.1:c.1816T>C	XP_024302932.1:p.Phe606Leu
XM_024447165.1:c.1183T>C	XP_024302933.1:p.Phe395Leu
NM_002485.5:c.2062T>C MANE Select	NP_002476.2:p.Phe688Leu
NM_001024688.3:c.1816T>C	NP_001019859.1:p.Phe606Leu