Canonical Allele Identifier: CA340877184

Gene: NEXN

Linked Data

• MyVariant Identifiers: chr1:g.78399135T>A (hg19) ; chr1:g.77933450T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77933450T>A , CM000663.2:g.77933450T>A	GRCh38
NC_000001.10:g.78399135T>A , CM000663.1:g.78399135T>A	GRCh37
NC_000001.9:g.78171723T>A	NCBI36
NG_016625.1:g.49936T>A , LRG_442:g.49936T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1222T>A MANE Select	ENSP00000333938.7:p.Phe408Ile
ENST00000330010.12:c.1030T>A	ENSP00000327363.8:p.Phe344Ile
ENST00000334785.11:c.1222T>A	ENSP00000333938.7:p.Phe408Ile
ENST00000342754.5:c.921T>A
ENST00000440324.5:c.1180T>A	ENSP00000411902.1:p.Phe394Ile
ENST00000464998.1:n.682T>A
ENST00000480732.2:n.796T>A
NM_001172309.1:c.1030T>A	NP_001165780.1:p.Phe344Ile
NM_144573.3:c.1222T>A , LRG_442t1:c.1222T>A	NP_653174.3:p.Phe408Ile
XM_005271322.2:c.1222T>A	XP_005271379.1:p.Phe408Ile
XM_005271323.2:c.1180T>A	XP_005271380.1:p.Phe394Ile
XM_005271324.3:c.1030T>A	XP_005271381.1:p.Phe344Ile
XM_005271325.2:c.1222T>A	XP_005271382.1:p.Phe408Ile
XM_005271326.2:c.988T>A	XP_005271383.1:p.Phe330Ile
XM_005271327.2:c.805T>A	XP_005271384.1:p.Phe269Ile
XM_005271322.4:c.1222T>A	XP_005271379.1:p.Phe408Ile
XM_005271323.4:c.1180T>A	XP_005271380.1:p.Phe394Ile
XM_005271324.5:c.1030T>A	XP_005271381.1:p.Phe344Ile
XM_005271325.4:c.1222T>A	XP_005271382.1:p.Phe408Ile
XM_005271326.4:c.988T>A	XP_005271383.1:p.Phe330Ile
XM_005271327.4:c.805T>A	XP_005271384.1:p.Phe269Ile
NM_001172309.2:c.1030T>A	NP_001165780.1:p.Phe344Ile
NM_144573.4:c.1222T>A MANE Select	NP_653174.3:p.Phe408Ile