Canonical Allele Identifier: CA1177631144

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942081T= , CM000663.2:g.77942081T=	GRCh38
NC_000001.10:g.78407766T= , CM000663.1:g.78407766T=	GRCh37
NC_000001.9:g.78180354T=	NCBI36
NG_016625.1:g.58567T= , LRG_442:g.58567T=
NG_033243.2:g.42013A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000334785.12:c.1532T= MANE Select	ENSP00000333938.7:p.Val511=
ENST00000330010.12:c.1340T=	ENSP00000327363.8:p.Val447=
ENST00000334785.11:c.1532T=	ENSP00000333938.7:p.Val511=
ENST00000342754.5:c.1231T=
ENST00000470735.1:n.371T=
ENST00000480732.2:n.1106T=
NM_001172309.1:c.1340T=	NP_001165780.1:p.Val447=
NM_144573.3:c.1532T= , LRG_442t1:c.1532T=	NP_653174.3:p.Val511=
XM_005271322.2:c.1532T=	XP_005271379.1:p.Val511=
XM_005271323.2:c.1490T=	XP_005271380.1:p.Val497=
XM_005271324.3:c.1340T=	XP_005271381.1:p.Val447=
XM_005271325.2:c.1310T=	XP_005271382.1:p.Val437=
XM_005271326.2:c.1298T=	XP_005271383.1:p.Val433=
XM_005271327.2:c.1115T=	XP_005271384.1:p.Val372=
XM_005271322.4:c.1532T=	XP_005271379.1:p.Val511=
XM_005271323.4:c.1490T=	XP_005271380.1:p.Val497=
XM_005271324.5:c.1340T=	XP_005271381.1:p.Val447=
XM_005271325.4:c.1310T=	XP_005271382.1:p.Val437=
XM_005271326.4:c.1298T=	XP_005271383.1:p.Val433=
XM_005271327.4:c.1115T=	XP_005271384.1:p.Val372=
NM_001172309.2:c.1340T=	NP_001165780.1:p.Val447=
NM_144573.4:c.1532T= MANE Select	NP_653174.3:p.Val511=