Canonical Allele Identifier: CA371676591

Gene: NBN

Linked Data

• MyVariant Identifiers: chr8:g.90958471A>G (hg19) ; chr8:g.89946243A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.89946243A>G , CM000670.2:g.89946243A>G	GRCh38
NC_000008.10:g.90958471A>G , CM000670.1:g.90958471A>G	GRCh37
NC_000008.9:g.91027647A>G	NCBI36
NG_008860.1:g.43429T>C , LRG_158:g.43429T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000494804.2:n.3269T>C
ENST00000517337.2:c.1721T>C	ENSP00000429971.2:p.Leu574Ser
ENST00000523444.2:c.1721T>C	ENSP00000428252.2:p.Leu574Ser
ENST00000697292.1:c.1967T>C	ENSP00000513229.1:p.Leu656Ser
ENST00000697293.1:c.1967T>C	ENSP00000513230.1:p.Leu656Ser
ENST00000697294.1:c.*1578T>C	ENSP00000513231.1:n.*1578T>C
ENST00000697295.1:c.*1276T>C	ENSP00000513232.1:n.*1276T>C
ENST00000697296.1:c.*1635T>C	ENSP00000513233.1:n.*1635T>C
ENST00000697297.1:n.3752T>C
ENST00000697298.1:c.1721T>C	ENSP00000513234.1:p.Leu574Ser
ENST00000697299.1:c.1721T>C	ENSP00000513235.1:p.Leu574Ser
ENST00000697300.1:c.*1571T>C	ENSP00000513236.1:n.*1571T>C
ENST00000697301.1:c.*1488T>C	ENSP00000513237.1:n.*1488T>C
ENST00000697302.1:c.*1488T>C	ENSP00000513238.1:n.*1488T>C
ENST00000697303.1:c.*1571T>C	ENSP00000513239.1:n.*1571T>C
ENST00000697304.1:c.1655T>C	ENSP00000513240.1:p.Leu552Ser
ENST00000697306.1:c.*2518T>C	ENSP00000513241.1:n.*2518T>C
ENST00000697307.1:c.1846-2877T>C	ENSP00000513242.1:n.1846-2877T>C
ENST00000697308.1:c.1898T>C	ENSP00000513243.1:p.Leu633Ser
ENST00000697309.1:c.1967T>C	ENSP00000513244.1:p.Leu656Ser
ENST00000697310.1:c.1967T>C	ENSP00000513245.1:p.Leu656Ser
ENST00000697311.1:c.1967T>C	ENSP00000513246.1:p.Leu656Ser
ENST00000697312.1:c.*1365T>C	ENSP00000513247.1:n.*1365T>C
ENST00000697313.1:n.2688-10631T>C
ENST00000697314.1:n.3636+7001T>C
ENST00000697315.1:c.1967T>C	ENSP00000513248.1:p.Leu656Ser
ENST00000697316.1:n.2088T>C
ENST00000697317.1:n.2058T>C
ENST00000265433.8:c.1967T>C MANE Select	ENSP00000265433.4:p.Leu656Ser
ENST00000265433.7:c.1967T>C	ENSP00000265433.3:p.Leu656Ser
ENST00000396252.6:c.*1840T>C	ENSP00000379551.2:n.*1840T>C
ENST00000409330.5:c.1721T>C	ENSP00000386924.1:p.Leu574Ser
ENST00000520325.1:n.383T>C
ENST00000613033.1:c.180+1581T>C	ENSP00000484487.1:n.180+1581T>C
NM_001024688.2:c.1721T>C	NP_001019859.1:p.Leu574Ser
NM_002485.4:c.1967T>C , LRG_158t1:c.1967T>C	NP_002476.2:p.Leu656Ser
XM_011517044.1:c.1943T>C	XP_011515346.1:p.Leu648Ser
XM_011517045.1:c.1721T>C	XP_011515347.1:p.Leu574Ser
XM_017013460.1:c.1088T>C	XP_016868949.1:p.Leu363Ser
XM_017013462.2:c.1088T>C	XP_016868951.1:p.Leu363Ser
XM_024447163.1:c.1721T>C	XP_024302931.1:p.Leu574Ser
XM_024447164.1:c.1721T>C	XP_024302932.1:p.Leu574Ser
XM_024447165.1:c.1088T>C	XP_024302933.1:p.Leu363Ser
NM_002485.5:c.1967T>C MANE Select	NP_002476.2:p.Leu656Ser
NM_001024688.3:c.1721T>C	NP_001019859.1:p.Leu574Ser