Canonical Allele Identifier: CA1177631158

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942114A= , CM000663.2:g.77942114A=	GRCh38
NC_000001.10:g.78407799A= , CM000663.1:g.78407799A=	GRCh37
NC_000001.9:g.78180387A=	NCBI36
NG_016625.1:g.58600A= , LRG_442:g.58600A=
NG_033243.2:g.41980T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000334785.12:c.1565A= MANE Select	ENSP00000333938.7:p.Lys522=
ENST00000330010.12:c.1373A=	ENSP00000327363.8:p.Lys458=
ENST00000334785.11:c.1565A=	ENSP00000333938.7:p.Lys522=
ENST00000342754.5:c.1264A=
ENST00000470735.1:n.404A=
ENST00000480732.2:n.1139A=
NM_001172309.1:c.1373A=	NP_001165780.1:p.Lys458=
NM_144573.3:c.1565A= , LRG_442t1:c.1565A=	NP_653174.3:p.Lys522=
XM_005271322.2:c.1565A=	XP_005271379.1:p.Lys522=
XM_005271323.2:c.1523A=	XP_005271380.1:p.Lys508=
XM_005271324.3:c.1373A=	XP_005271381.1:p.Lys458=
XM_005271325.2:c.1343A=	XP_005271382.1:p.Lys448=
XM_005271326.2:c.1331A=	XP_005271383.1:p.Lys444=
XM_005271327.2:c.1148A=	XP_005271384.1:p.Lys383=
XM_005271322.4:c.1565A=	XP_005271379.1:p.Lys522=
XM_005271323.4:c.1523A=	XP_005271380.1:p.Lys508=
XM_005271324.5:c.1373A=	XP_005271381.1:p.Lys458=
XM_005271325.4:c.1343A=	XP_005271382.1:p.Lys448=
XM_005271326.4:c.1331A=	XP_005271383.1:p.Lys444=
XM_005271327.4:c.1148A=	XP_005271384.1:p.Lys383=
NM_001172309.2:c.1373A=	NP_001165780.1:p.Lys458=
NM_144573.4:c.1565A= MANE Select	NP_653174.3:p.Lys522=