Canonical Allele Identifier: CA1143388511

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77935887G= , CM000663.2:g.77935887G=	GRCh38
NC_000001.10:g.78401572G= , CM000663.1:g.78401572G=	GRCh37
NC_000001.9:g.78174160G=	NCBI36
NG_016625.1:g.52373G= , LRG_442:g.52373G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1316G= MANE Select	ENSP00000333938.7:p.Arg439=
ENST00000330010.12:c.1124G=	ENSP00000327363.8:p.Arg375=
ENST00000334785.11:c.1316G=	ENSP00000333938.7:p.Arg439=
ENST00000342754.5:c.1015G=
ENST00000440324.5:c.1274G=	ENSP00000411902.1:p.Arg425=
ENST00000464998.1:n.776G=
ENST00000480732.2:n.890G=
NM_001172309.1:c.1124G=	NP_001165780.1:p.Arg375=
NM_144573.3:c.1316G= , LRG_442t1:c.1316G=	NP_653174.3:p.Arg439=
XM_005271322.2:c.1316G=	XP_005271379.1:p.Arg439=
XM_005271323.2:c.1274G=	XP_005271380.1:p.Arg425=
XM_005271324.3:c.1124G=	XP_005271381.1:p.Arg375=
XM_005271325.2:c.1251+2408G=	XP_005271382.1:n.1251+2408G=
XM_005271326.2:c.1082G=	XP_005271383.1:p.Arg361=
XM_005271327.2:c.899G=	XP_005271384.1:p.Arg300=
XM_005271322.4:c.1316G=	XP_005271379.1:p.Arg439=
XM_005271323.4:c.1274G=	XP_005271380.1:p.Arg425=
XM_005271324.5:c.1124G=	XP_005271381.1:p.Arg375=
XM_005271325.4:c.1251+2408G=	XP_005271382.1:n.1251+2408G=
XM_005271326.4:c.1082G=	XP_005271383.1:p.Arg361=
XM_005271327.4:c.899G=	XP_005271384.1:p.Arg300=
NM_001172309.2:c.1124G=	NP_001165780.1:p.Arg375=
NM_144573.4:c.1316G= MANE Select	NP_653174.3:p.Arg439=