Canonical Allele Identifier: CA1177628332

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77935988A= , CM000663.2:g.77935988A=	GRCh38
NC_000001.10:g.78401673A= , CM000663.1:g.78401673A=	GRCh37
NC_000001.9:g.78174261A=	NCBI36
NG_016625.1:g.52474A= , LRG_442:g.52474A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000334785.12:c.1417A= MANE Select	ENSP00000333938.7:p.Arg473=
ENST00000330010.12:c.1225A=	ENSP00000327363.8:p.Arg409=
ENST00000334785.11:c.1417A=	ENSP00000333938.7:p.Arg473=
ENST00000342754.5:c.1116A=
ENST00000480732.2:n.991A=
NM_001172309.1:c.1225A=	NP_001165780.1:p.Arg409=
NM_144573.3:c.1417A= , LRG_442t1:c.1417A=	NP_653174.3:p.Arg473=
XM_005271322.2:c.1417A=	XP_005271379.1:p.Arg473=
XM_005271323.2:c.1375A=	XP_005271380.1:p.Arg459=
XM_005271324.3:c.1225A=	XP_005271381.1:p.Arg409=
XM_005271325.2:c.1251+2509A=	XP_005271382.1:n.1251+2509A=
XM_005271326.2:c.1183A=	XP_005271383.1:p.Arg395=
XM_005271327.2:c.1000A=	XP_005271384.1:p.Arg334=
XM_005271322.4:c.1417A=	XP_005271379.1:p.Arg473=
XM_005271323.4:c.1375A=	XP_005271380.1:p.Arg459=
XM_005271324.5:c.1225A=	XP_005271381.1:p.Arg409=
XM_005271325.4:c.1251+2509A=	XP_005271382.1:n.1251+2509A=
XM_005271326.4:c.1183A=	XP_005271383.1:p.Arg395=
XM_005271327.4:c.1000A=	XP_005271384.1:p.Arg334=
NM_001172309.2:c.1225A=	NP_001165780.1:p.Arg409=
NM_144573.4:c.1417A= MANE Select	NP_653174.3:p.Arg473=