Canonical Allele Identifier: CA1148224378

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942077A= , CM000663.2:g.77942077A=	GRCh38
NC_000001.10:g.78407762A= , CM000663.1:g.78407762A=	GRCh37
NC_000001.9:g.78180350A=	NCBI36
NG_016625.1:g.58563A= , LRG_442:g.58563A=
NG_033243.2:g.42017T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000334785.12:c.1528A= MANE Select	ENSP00000333938.7:p.Lys510=
ENST00000330010.12:c.1336A=	ENSP00000327363.8:p.Lys446=
ENST00000334785.11:c.1528A=	ENSP00000333938.7:p.Lys510=
ENST00000342754.5:c.1227A=
ENST00000470735.1:n.367A=
ENST00000480732.2:n.1102A=
NM_001172309.1:c.1336A=	NP_001165780.1:p.Lys446=
NM_144573.3:c.1528A= , LRG_442t1:c.1528A=	NP_653174.3:p.Lys510=
XM_005271322.2:c.1528A=	XP_005271379.1:p.Lys510=
XM_005271323.2:c.1486A=	XP_005271380.1:p.Lys496=
XM_005271324.3:c.1336A=	XP_005271381.1:p.Lys446=
XM_005271325.2:c.1306A=	XP_005271382.1:p.Lys436=
XM_005271326.2:c.1294A=	XP_005271383.1:p.Lys432=
XM_005271327.2:c.1111A=	XP_005271384.1:p.Lys371=
XM_005271322.4:c.1528A=	XP_005271379.1:p.Lys510=
XM_005271323.4:c.1486A=	XP_005271380.1:p.Lys496=
XM_005271324.5:c.1336A=	XP_005271381.1:p.Lys446=
XM_005271325.4:c.1306A=	XP_005271382.1:p.Lys436=
XM_005271326.4:c.1294A=	XP_005271383.1:p.Lys432=
XM_005271327.4:c.1111A=	XP_005271384.1:p.Lys371=
NM_001172309.2:c.1336A=	NP_001165780.1:p.Lys446=
NM_144573.4:c.1528A= MANE Select	NP_653174.3:p.Lys510=