Canonical Allele Identifier: CA918733

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77926817G>A , CM000663.2:g.77926817G>A	GRCh38
NC_000001.10:g.78392502G>A , CM000663.1:g.78392502G>A	GRCh37
NC_000001.9:g.78165090G>A	NCBI36
NG_016625.1:g.43303G>A , LRG_442:g.43303G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_144573.4:c.789G>A MANE Select	NP_653174.3:p.Lys263=
ENST00000334785.12:c.789G>A MANE Select	ENSP00000333938.7:p.Lys263=
NM_001172309.1:c.597G>A	NP_001165780.1:p.Lys199=
NM_001172309.2:c.597G>A	NP_001165780.1:p.Lys199=
NM_144573.3:c.789G>A , LRG_442t1:c.789G>A	NP_653174.3:p.Lys263=
ENST00000330010.12:c.597G>A	ENSP00000327363.8:p.Lys199=
ENST00000334785.11:c.789G>A	ENSP00000333938.7:p.Lys263=
ENST00000342754.5:c.488G>A
ENST00000401035.7:c.597G>A	ENSP00000383814.3:p.Lys199=
ENST00000440324.5:c.747G>A	ENSP00000411902.1:p.Lys249=
ENST00000464998.1:n.249G>A
XM_005271322.2:c.789G>A	XP_005271379.1:p.Lys263=
XM_005271322.4:c.789G>A	XP_005271379.1:p.Lys263=
XM_005271323.2:c.747G>A	XP_005271380.1:p.Lys249=
XM_005271323.4:c.747G>A	XP_005271380.1:p.Lys249=
XM_005271324.3:c.597G>A	XP_005271381.1:p.Lys199=
XM_005271324.5:c.597G>A	XP_005271381.1:p.Lys199=
XM_005271325.2:c.789G>A	XP_005271382.1:p.Lys263=
XM_005271325.4:c.789G>A	XP_005271382.1:p.Lys263=
XM_005271326.2:c.555G>A	XP_005271383.1:p.Lys185=
XM_005271326.4:c.555G>A	XP_005271383.1:p.Lys185=
XM_005271327.2:c.448-2499G>A	XP_005271384.1:n.448-2499G>A
XM_005271327.4:c.448-2499G>A	XP_005271384.1:n.448-2499G>A