Canonical Allele Identifier: CA1177631153

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942102A= , CM000663.2:g.77942102A=	GRCh38
NC_000001.10:g.78407787A= , CM000663.1:g.78407787A=	GRCh37
NC_000001.9:g.78180375A=	NCBI36
NG_016625.1:g.58588A= , LRG_442:g.58588A=
NG_033243.2:g.41992T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000334785.12:c.1553A= MANE Select	ENSP00000333938.7:p.Glu518=
ENST00000330010.12:c.1361A=	ENSP00000327363.8:p.Glu454=
ENST00000334785.11:c.1553A=	ENSP00000333938.7:p.Glu518=
ENST00000342754.5:c.1252A=
ENST00000470735.1:n.392A=
ENST00000480732.2:n.1127A=
NM_001172309.1:c.1361A=	NP_001165780.1:p.Glu454=
NM_144573.3:c.1553A= , LRG_442t1:c.1553A=	NP_653174.3:p.Glu518=
XM_005271322.2:c.1553A=	XP_005271379.1:p.Glu518=
XM_005271323.2:c.1511A=	XP_005271380.1:p.Glu504=
XM_005271324.3:c.1361A=	XP_005271381.1:p.Glu454=
XM_005271325.2:c.1331A=	XP_005271382.1:p.Glu444=
XM_005271326.2:c.1319A=	XP_005271383.1:p.Glu440=
XM_005271327.2:c.1136A=	XP_005271384.1:p.Glu379=
XM_005271322.4:c.1553A=	XP_005271379.1:p.Glu518=
XM_005271323.4:c.1511A=	XP_005271380.1:p.Glu504=
XM_005271324.5:c.1361A=	XP_005271381.1:p.Glu454=
XM_005271325.4:c.1331A=	XP_005271382.1:p.Glu444=
XM_005271326.4:c.1319A=	XP_005271383.1:p.Glu440=
XM_005271327.4:c.1136A=	XP_005271384.1:p.Glu379=
NM_001172309.2:c.1361A=	NP_001165780.1:p.Glu454=
NM_144573.4:c.1553A= MANE Select	NP_653174.3:p.Glu518=