Canonical Allele Identifier: CA1177626169

Gene: NEXN

Linked Data

• dbSNP Id: rs1651505944

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942848A>G , CM000663.2:g.77942848A>G	GRCh38
NC_000001.10:g.78408533A>G , CM000663.1:g.78408533A>G	GRCh37
NC_000001.9:g.78181121A>G	NCBI36
NG_016625.1:g.59334A>G , LRG_442:g.59334A>G
NG_033243.2:g.41246T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.*19A>G MANE Select	ENSP00000333938.7:n.*19A>G
ENST00000330010.12:c.*19A>G	ENSP00000327363.8:n.*19A>G
ENST00000334785.11:c.*19A>G	ENSP00000333938.7:n.*19A>G
ENST00000342754.5:c.1716+30A>G
ENST00000480732.2:n.1621A>G
NM_001172309.1:c.*19A>G	NP_001165780.1:n.*19A>G
NM_144573.3:c.*19A>G , LRG_442t1:c.*19A>G	NP_653174.3:n.*19A>G
XM_005271322.2:c.2017+30A>G	XP_005271379.1:n.2017+30A>G
XM_005271323.2:c.1975+30A>G	XP_005271380.1:n.1975+30A>G
XM_005271324.3:c.1825+30A>G	XP_005271381.1:n.1825+30A>G
XM_005271325.2:c.1795+30A>G	XP_005271382.1:n.1795+30A>G
XM_005271326.2:c.1783+30A>G	XP_005271383.1:n.1783+30A>G
XM_005271327.2:c.1600+30A>G	XP_005271384.1:n.1600+30A>G
XM_005271322.4:c.2017+30A>G	XP_005271379.1:n.2017+30A>G
XM_005271323.4:c.1975+30A>G	XP_005271380.1:n.1975+30A>G
XM_005271324.5:c.1825+30A>G	XP_005271381.1:n.1825+30A>G
XM_005271325.4:c.1795+30A>G	XP_005271382.1:n.1795+30A>G
XM_005271326.4:c.1783+30A>G	XP_005271383.1:n.1783+30A>G
XM_005271327.4:c.1600+30A>G	XP_005271384.1:n.1600+30A>G
NM_001172309.2:c.*19A>G	NP_001165780.1:n.*19A>G
NM_144573.4:c.*19A>G MANE Select	NP_653174.3:n.*19A>G