Canonical Allele Identifier: CA1177628292

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77935899T= , CM000663.2:g.77935899T=	GRCh38
NC_000001.10:g.78401584T= , CM000663.1:g.78401584T=	GRCh37
NC_000001.9:g.78174172T=	NCBI36
NG_016625.1:g.52385T= , LRG_442:g.52385T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1328T= MANE Select	ENSP00000333938.7:p.Ile443=
ENST00000330010.12:c.1136T=	ENSP00000327363.8:p.Ile379=
ENST00000334785.11:c.1328T=	ENSP00000333938.7:p.Ile443=
ENST00000342754.5:c.1027T=
ENST00000440324.5:c.1286T=	ENSP00000411902.1:p.Ile429=
ENST00000464998.1:n.788T=
ENST00000480732.2:n.902T=
NM_001172309.1:c.1136T=	NP_001165780.1:p.Ile379=
NM_144573.3:c.1328T= , LRG_442t1:c.1328T=	NP_653174.3:p.Ile443=
XM_005271322.2:c.1328T=	XP_005271379.1:p.Ile443=
XM_005271323.2:c.1286T=	XP_005271380.1:p.Ile429=
XM_005271324.3:c.1136T=	XP_005271381.1:p.Ile379=
XM_005271325.2:c.1251+2420T=	XP_005271382.1:n.1251+2420T=
XM_005271326.2:c.1094T=	XP_005271383.1:p.Ile365=
XM_005271327.2:c.911T=	XP_005271384.1:p.Ile304=
XM_005271322.4:c.1328T=	XP_005271379.1:p.Ile443=
XM_005271323.4:c.1286T=	XP_005271380.1:p.Ile429=
XM_005271324.5:c.1136T=	XP_005271381.1:p.Ile379=
XM_005271325.4:c.1251+2420T=	XP_005271382.1:n.1251+2420T=
XM_005271326.4:c.1094T=	XP_005271383.1:p.Ile365=
XM_005271327.4:c.911T=	XP_005271384.1:p.Ile304=
NM_001172309.2:c.1136T=	NP_001165780.1:p.Ile379=
NM_144573.4:c.1328T= MANE Select	NP_653174.3:p.Ile443=