Canonical Allele Identifier: CA340881157

Gene: NEXN

Linked Data

• gnomAD v4: 1-77942125-G-A
• MyVariant Identifiers: chr1:g.78407810G>A (hg19) ; chr1:g.77942125G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942125G>A , CM000663.2:g.77942125G>A	GRCh38
NC_000001.10:g.78407810G>A , CM000663.1:g.78407810G>A	GRCh37
NC_000001.9:g.78180398G>A	NCBI36
NG_016625.1:g.58611G>A , LRG_442:g.58611G>A
NG_033243.2:g.41969C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000334785.12:c.1576G>A MANE Select	ENSP00000333938.7:p.Glu526Lys
ENST00000330010.12:c.1384G>A	ENSP00000327363.8:p.Glu462Lys
ENST00000334785.11:c.1576G>A	ENSP00000333938.7:p.Glu526Lys
ENST00000342754.5:c.1275G>A
ENST00000470735.1:n.415G>A
ENST00000480732.2:n.1150G>A
NM_001172309.1:c.1384G>A	NP_001165780.1:p.Glu462Lys
NM_144573.3:c.1576G>A , LRG_442t1:c.1576G>A	NP_653174.3:p.Glu526Lys
XM_005271322.2:c.1576G>A	XP_005271379.1:p.Glu526Lys
XM_005271323.2:c.1534G>A	XP_005271380.1:p.Glu512Lys
XM_005271324.3:c.1384G>A	XP_005271381.1:p.Glu462Lys
XM_005271325.2:c.1354G>A	XP_005271382.1:p.Glu452Lys
XM_005271326.2:c.1342G>A	XP_005271383.1:p.Glu448Lys
XM_005271327.2:c.1159G>A	XP_005271384.1:p.Glu387Lys
XM_005271322.4:c.1576G>A	XP_005271379.1:p.Glu526Lys
XM_005271323.4:c.1534G>A	XP_005271380.1:p.Glu512Lys
XM_005271324.5:c.1384G>A	XP_005271381.1:p.Glu462Lys
XM_005271325.4:c.1354G>A	XP_005271382.1:p.Glu452Lys
XM_005271326.4:c.1342G>A	XP_005271383.1:p.Glu448Lys
XM_005271327.4:c.1159G>A	XP_005271384.1:p.Glu387Lys
NM_001172309.2:c.1384G>A	NP_001165780.1:p.Glu462Lys
NM_144573.4:c.1576G>A MANE Select	NP_653174.3:p.Glu526Lys