Canonical Allele Identifier: CA1177623614

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77926269A= , CM000663.2:g.77926269A=	GRCh38
NC_000001.10:g.78391954A= , CM000663.1:g.78391954A=	GRCh37
NC_000001.9:g.78164542A=	NCBI36
NG_016625.1:g.42755A= , LRG_442:g.42755A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.490-145A= MANE Select	ENSP00000333938.7:n.490-145A=
ENST00000330010.12:c.298-145A=	ENSP00000327363.8:n.298-145A=
ENST00000334785.11:c.490-145A=	ENSP00000333938.7:n.490-145A=
ENST00000342754.5:c.189-145A=
ENST00000401035.7:c.298-145A=	ENSP00000383814.3:n.298-145A=
ENST00000440324.5:c.448-145A=	ENSP00000411902.1:n.448-145A=
NM_001172309.1:c.298-145A=	NP_001165780.1:n.298-145A=
NM_144573.3:c.490-145A= , LRG_442t1:c.490-145A=	NP_653174.3:n.490-145A=
XM_005271322.2:c.490-145A=	XP_005271379.1:n.490-145A=
XM_005271323.2:c.448-145A=	XP_005271380.1:n.448-145A=
XM_005271324.3:c.298-145A=	XP_005271381.1:n.298-145A=
XM_005271325.2:c.490-145A=	XP_005271382.1:n.490-145A=
XM_005271326.2:c.256-145A=	XP_005271383.1:n.256-145A=
XM_005271327.2:c.448-3047A=	XP_005271384.1:n.448-3047A=
XM_005271322.4:c.490-145A=	XP_005271379.1:n.490-145A=
XM_005271323.4:c.448-145A=	XP_005271380.1:n.448-145A=
XM_005271324.5:c.298-145A=	XP_005271381.1:n.298-145A=
XM_005271325.4:c.490-145A=	XP_005271382.1:n.490-145A=
XM_005271326.4:c.256-145A=	XP_005271383.1:n.256-145A=
XM_005271327.4:c.448-3047A=	XP_005271384.1:n.448-3047A=
NM_001172309.2:c.298-145A=	NP_001165780.1:n.298-145A=
NM_144573.4:c.490-145A= MANE Select	NP_653174.3:n.490-145A=