Canonical Allele Identifier: CA340881685

Gene: NEXN

Linked Data

• MyVariant Identifiers: chr1:g.78407892A>T (hg19) ; chr1:g.77942207A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942207A>T , CM000663.2:g.77942207A>T	GRCh38
NC_000001.10:g.78407892A>T , CM000663.1:g.78407892A>T	GRCh37
NC_000001.9:g.78180480A>T	NCBI36
NG_016625.1:g.58693A>T , LRG_442:g.58693A>T
NG_033243.2:g.41887T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000334785.12:c.1658A>T MANE Select	ENSP00000333938.7:p.Lys553Met
ENST00000330010.12:c.1466A>T	ENSP00000327363.8:p.Lys489Met
ENST00000334785.11:c.1658A>T	ENSP00000333938.7:p.Lys553Met
ENST00000342754.5:c.1357A>T
ENST00000470735.1:n.497A>T
ENST00000480732.2:n.1232A>T
NM_001172309.1:c.1466A>T	NP_001165780.1:p.Lys489Met
NM_144573.3:c.1658A>T , LRG_442t1:c.1658A>T	NP_653174.3:p.Lys553Met
XM_005271322.2:c.1658A>T	XP_005271379.1:p.Lys553Met
XM_005271323.2:c.1616A>T	XP_005271380.1:p.Lys539Met
XM_005271324.3:c.1466A>T	XP_005271381.1:p.Lys489Met
XM_005271325.2:c.1436A>T	XP_005271382.1:p.Lys479Met
XM_005271326.2:c.1424A>T	XP_005271383.1:p.Lys475Met
XM_005271327.2:c.1241A>T	XP_005271384.1:p.Lys414Met
XM_005271322.4:c.1658A>T	XP_005271379.1:p.Lys553Met
XM_005271323.4:c.1616A>T	XP_005271380.1:p.Lys539Met
XM_005271324.5:c.1466A>T	XP_005271381.1:p.Lys489Met
XM_005271325.4:c.1436A>T	XP_005271382.1:p.Lys479Met
XM_005271326.4:c.1424A>T	XP_005271383.1:p.Lys475Met
XM_005271327.4:c.1241A>T	XP_005271384.1:p.Lys414Met
NM_001172309.2:c.1466A>T	NP_001165780.1:p.Lys489Met
NM_144573.4:c.1658A>T MANE Select	NP_653174.3:p.Lys553Met