Canonical Allele Identifier: CA1177628326

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77935974A= , CM000663.2:g.77935974A=	GRCh38
NC_000001.10:g.78401659A= , CM000663.1:g.78401659A=	GRCh37
NC_000001.9:g.78174247A=	NCBI36
NG_016625.1:g.52460A= , LRG_442:g.52460A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1403A= MANE Select	ENSP00000333938.7:p.Glu468=
ENST00000330010.12:c.1211A=	ENSP00000327363.8:p.Glu404=
ENST00000334785.11:c.1403A=	ENSP00000333938.7:p.Glu468=
ENST00000342754.5:c.1102A=
ENST00000480732.2:n.977A=
NM_001172309.1:c.1211A=	NP_001165780.1:p.Glu404=
NM_144573.3:c.1403A= , LRG_442t1:c.1403A=	NP_653174.3:p.Glu468=
XM_005271322.2:c.1403A=	XP_005271379.1:p.Glu468=
XM_005271323.2:c.1361A=	XP_005271380.1:p.Glu454=
XM_005271324.3:c.1211A=	XP_005271381.1:p.Glu404=
XM_005271325.2:c.1251+2495A=	XP_005271382.1:n.1251+2495A=
XM_005271326.2:c.1169A=	XP_005271383.1:p.Glu390=
XM_005271327.2:c.986A=	XP_005271384.1:p.Glu329=
XM_005271322.4:c.1403A=	XP_005271379.1:p.Glu468=
XM_005271323.4:c.1361A=	XP_005271380.1:p.Glu454=
XM_005271324.5:c.1211A=	XP_005271381.1:p.Glu404=
XM_005271325.4:c.1251+2495A=	XP_005271382.1:n.1251+2495A=
XM_005271326.4:c.1169A=	XP_005271383.1:p.Glu390=
XM_005271327.4:c.986A=	XP_005271384.1:p.Glu329=
NM_001172309.2:c.1211A=	NP_001165780.1:p.Glu404=
NM_144573.4:c.1403A= MANE Select	NP_653174.3:p.Glu468=