Canonical Allele Identifier: CA340878822

Gene: NEXN

Linked Data

• MyVariant Identifiers: chr1:g.78401599T>A (hg19) ; chr1:g.77935914T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77935914T>A , CM000663.2:g.77935914T>A	GRCh38
NC_000001.10:g.78401599T>A , CM000663.1:g.78401599T>A	GRCh37
NC_000001.9:g.78174187T>A	NCBI36
NG_016625.1:g.52400T>A , LRG_442:g.52400T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1343T>A MANE Select	ENSP00000333938.7:p.Leu448Gln
ENST00000330010.12:c.1151T>A	ENSP00000327363.8:p.Leu384Gln
ENST00000334785.11:c.1343T>A	ENSP00000333938.7:p.Leu448Gln
ENST00000342754.5:c.1042T>A
ENST00000440324.5:c.1301T>A	ENSP00000411902.1:p.Leu434Gln
ENST00000464998.1:n.803T>A
ENST00000480732.2:n.917T>A
NM_001172309.1:c.1151T>A	NP_001165780.1:p.Leu384Gln
NM_144573.3:c.1343T>A , LRG_442t1:c.1343T>A	NP_653174.3:p.Leu448Gln
XM_005271322.2:c.1343T>A	XP_005271379.1:p.Leu448Gln
XM_005271323.2:c.1301T>A	XP_005271380.1:p.Leu434Gln
XM_005271324.3:c.1151T>A	XP_005271381.1:p.Leu384Gln
XM_005271325.2:c.1251+2435T>A	XP_005271382.1:n.1251+2435T>A
XM_005271326.2:c.1109T>A	XP_005271383.1:p.Leu370Gln
XM_005271327.2:c.926T>A	XP_005271384.1:p.Leu309Gln
XM_005271322.4:c.1343T>A	XP_005271379.1:p.Leu448Gln
XM_005271323.4:c.1301T>A	XP_005271380.1:p.Leu434Gln
XM_005271324.5:c.1151T>A	XP_005271381.1:p.Leu384Gln
XM_005271325.4:c.1251+2435T>A	XP_005271382.1:n.1251+2435T>A
XM_005271326.4:c.1109T>A	XP_005271383.1:p.Leu370Gln
XM_005271327.4:c.926T>A	XP_005271384.1:p.Leu309Gln
NM_001172309.2:c.1151T>A	NP_001165780.1:p.Leu384Gln
NM_144573.4:c.1343T>A MANE Select	NP_653174.3:p.Leu448Gln