Canonical Allele Identifier: CA1177623650

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77926362A= , CM000663.2:g.77926362A=	GRCh38
NC_000001.10:g.78392047A= , CM000663.1:g.78392047A=	GRCh37
NC_000001.9:g.78164635A=	NCBI36
NG_016625.1:g.42848A= , LRG_442:g.42848A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000334785.12:c.490-52A= MANE Select	ENSP00000333938.7:n.490-52A=
ENST00000330010.12:c.298-52A=	ENSP00000327363.8:n.298-52A=
ENST00000334785.11:c.490-52A=	ENSP00000333938.7:n.490-52A=
ENST00000342754.5:c.189-52A=
ENST00000401035.7:c.298-52A=	ENSP00000383814.3:n.298-52A=
ENST00000440324.5:c.448-52A=	ENSP00000411902.1:n.448-52A=
NM_001172309.1:c.298-52A=	NP_001165780.1:n.298-52A=
NM_144573.3:c.490-52A= , LRG_442t1:c.490-52A=	NP_653174.3:n.490-52A=
XM_005271322.2:c.490-52A=	XP_005271379.1:n.490-52A=
XM_005271323.2:c.448-52A=	XP_005271380.1:n.448-52A=
XM_005271324.3:c.298-52A=	XP_005271381.1:n.298-52A=
XM_005271325.2:c.490-52A=	XP_005271382.1:n.490-52A=
XM_005271326.2:c.256-52A=	XP_005271383.1:n.256-52A=
XM_005271327.2:c.448-2954A=	XP_005271384.1:n.448-2954A=
XM_005271322.4:c.490-52A=	XP_005271379.1:n.490-52A=
XM_005271323.4:c.448-52A=	XP_005271380.1:n.448-52A=
XM_005271324.5:c.298-52A=	XP_005271381.1:n.298-52A=
XM_005271325.4:c.490-52A=	XP_005271382.1:n.490-52A=
XM_005271326.4:c.256-52A=	XP_005271383.1:n.256-52A=
XM_005271327.4:c.448-2954A=	XP_005271384.1:n.448-2954A=
NM_001172309.2:c.298-52A=	NP_001165780.1:n.298-52A=
NM_144573.4:c.490-52A= MANE Select	NP_653174.3:n.490-52A=