Canonical Allele Identifier: CA340881167

Gene: NEXN

Linked Data

• MyVariant Identifiers: chr1:g.78407812A>T (hg19) ; chr1:g.77942127A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942127A>T , CM000663.2:g.77942127A>T	GRCh38
NC_000001.10:g.78407812A>T , CM000663.1:g.78407812A>T	GRCh37
NC_000001.9:g.78180400A>T	NCBI36
NG_016625.1:g.58613A>T , LRG_442:g.58613A>T
NG_033243.2:g.41967T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1578A>T MANE Select	ENSP00000333938.7:p.Glu526Asp
ENST00000330010.12:c.1386A>T	ENSP00000327363.8:p.Glu462Asp
ENST00000334785.11:c.1578A>T	ENSP00000333938.7:p.Glu526Asp
ENST00000342754.5:c.1277A>T
ENST00000470735.1:n.417A>T
ENST00000480732.2:n.1152A>T
NM_001172309.1:c.1386A>T	NP_001165780.1:p.Glu462Asp
NM_144573.3:c.1578A>T , LRG_442t1:c.1578A>T	NP_653174.3:p.Glu526Asp
XM_005271322.2:c.1578A>T	XP_005271379.1:p.Glu526Asp
XM_005271323.2:c.1536A>T	XP_005271380.1:p.Glu512Asp
XM_005271324.3:c.1386A>T	XP_005271381.1:p.Glu462Asp
XM_005271325.2:c.1356A>T	XP_005271382.1:p.Glu452Asp
XM_005271326.2:c.1344A>T	XP_005271383.1:p.Glu448Asp
XM_005271327.2:c.1161A>T	XP_005271384.1:p.Glu387Asp
XM_005271322.4:c.1578A>T	XP_005271379.1:p.Glu526Asp
XM_005271323.4:c.1536A>T	XP_005271380.1:p.Glu512Asp
XM_005271324.5:c.1386A>T	XP_005271381.1:p.Glu462Asp
XM_005271325.4:c.1356A>T	XP_005271382.1:p.Glu452Asp
XM_005271326.4:c.1344A>T	XP_005271383.1:p.Glu448Asp
XM_005271327.4:c.1161A>T	XP_005271384.1:p.Glu387Asp
NM_001172309.2:c.1386A>T	NP_001165780.1:p.Glu462Asp
NM_144573.4:c.1578A>T MANE Select	NP_653174.3:p.Glu526Asp