Canonical Allele Identifier: CA1177624779

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77929230T= , CM000663.2:g.77929230T=	GRCh38
NC_000001.10:g.78394915T= , CM000663.1:g.78394915T=	GRCh37
NC_000001.9:g.78167503T=	NCBI36
NG_016625.1:g.45716T= , LRG_442:g.45716T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000334785.12:c.865-86T= MANE Select	ENSP00000333938.7:n.865-86T=
ENST00000330010.12:c.673-86T=	ENSP00000327363.8:n.673-86T=
ENST00000334785.11:c.865-86T=	ENSP00000333938.7:n.865-86T=
ENST00000342754.5:c.564-86T=
ENST00000401035.7:c.673-86T=	ENSP00000383814.3:n.673-86T=
ENST00000440324.5:c.823-86T=	ENSP00000411902.1:n.823-86T=
ENST00000464998.1:n.325-86T=
NM_001172309.1:c.673-86T=	NP_001165780.1:n.673-86T=
NM_144573.3:c.865-86T= , LRG_442t1:c.865-86T=	NP_653174.3:n.865-86T=
XM_005271322.2:c.865-86T=	XP_005271379.1:n.865-86T=
XM_005271323.2:c.823-86T=	XP_005271380.1:n.823-86T=
XM_005271324.3:c.673-86T=	XP_005271381.1:n.673-86T=
XM_005271325.2:c.865-86T=	XP_005271382.1:n.865-86T=
XM_005271326.2:c.631-86T=	XP_005271383.1:n.631-86T=
XM_005271327.2:c.448-86T=	XP_005271384.1:n.448-86T=
XM_005271322.4:c.865-86T=	XP_005271379.1:n.865-86T=
XM_005271323.4:c.823-86T=	XP_005271380.1:n.823-86T=
XM_005271324.5:c.673-86T=	XP_005271381.1:n.673-86T=
XM_005271325.4:c.865-86T=	XP_005271382.1:n.865-86T=
XM_005271326.4:c.631-86T=	XP_005271383.1:n.631-86T=
XM_005271327.4:c.448-86T=	XP_005271384.1:n.448-86T=
NM_001172309.2:c.673-86T=	NP_001165780.1:n.673-86T=
NM_144573.4:c.865-86T= MANE Select	NP_653174.3:n.865-86T=