Canonical Allele Identifier: CA1177628330

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77935984A= , CM000663.2:g.77935984A=	GRCh38
NC_000001.10:g.78401669A= , CM000663.1:g.78401669A=	GRCh37
NC_000001.9:g.78174257A=	NCBI36
NG_016625.1:g.52470A= , LRG_442:g.52470A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000334785.12:c.1413A= MANE Select	ENSP00000333938.7:p.Arg471=
ENST00000330010.12:c.1221A=	ENSP00000327363.8:p.Arg407=
ENST00000334785.11:c.1413A=	ENSP00000333938.7:p.Arg471=
ENST00000342754.5:c.1112A=
ENST00000480732.2:n.987A=
NM_001172309.1:c.1221A=	NP_001165780.1:p.Arg407=
NM_144573.3:c.1413A= , LRG_442t1:c.1413A=	NP_653174.3:p.Arg471=
XM_005271322.2:c.1413A=	XP_005271379.1:p.Arg471=
XM_005271323.2:c.1371A=	XP_005271380.1:p.Arg457=
XM_005271324.3:c.1221A=	XP_005271381.1:p.Arg407=
XM_005271325.2:c.1251+2505A=	XP_005271382.1:n.1251+2505A=
XM_005271326.2:c.1179A=	XP_005271383.1:p.Arg393=
XM_005271327.2:c.996A=	XP_005271384.1:p.Arg332=
XM_005271322.4:c.1413A=	XP_005271379.1:p.Arg471=
XM_005271323.4:c.1371A=	XP_005271380.1:p.Arg457=
XM_005271324.5:c.1221A=	XP_005271381.1:p.Arg407=
XM_005271325.4:c.1251+2505A=	XP_005271382.1:n.1251+2505A=
XM_005271326.4:c.1179A=	XP_005271383.1:p.Arg393=
XM_005271327.4:c.996A=	XP_005271384.1:p.Arg332=
NM_001172309.2:c.1221A=	NP_001165780.1:p.Arg407=
NM_144573.4:c.1413A= MANE Select	NP_653174.3:p.Arg471=