Canonical Allele Identifier: CA1177628296

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77935908A= , CM000663.2:g.77935908A=	GRCh38
NC_000001.10:g.78401593A= , CM000663.1:g.78401593A=	GRCh37
NC_000001.9:g.78174181A=	NCBI36
NG_016625.1:g.52394A= , LRG_442:g.52394A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1337A= MANE Select	ENSP00000333938.7:p.Lys446=
ENST00000330010.12:c.1145A=	ENSP00000327363.8:p.Lys382=
ENST00000334785.11:c.1337A=	ENSP00000333938.7:p.Lys446=
ENST00000342754.5:c.1036A=
ENST00000440324.5:c.1295A=	ENSP00000411902.1:p.Lys432=
ENST00000464998.1:n.797A=
ENST00000480732.2:n.911A=
NM_001172309.1:c.1145A=	NP_001165780.1:p.Lys382=
NM_144573.3:c.1337A= , LRG_442t1:c.1337A=	NP_653174.3:p.Lys446=
XM_005271322.2:c.1337A=	XP_005271379.1:p.Lys446=
XM_005271323.2:c.1295A=	XP_005271380.1:p.Lys432=
XM_005271324.3:c.1145A=	XP_005271381.1:p.Lys382=
XM_005271325.2:c.1251+2429A=	XP_005271382.1:n.1251+2429A=
XM_005271326.2:c.1103A=	XP_005271383.1:p.Lys368=
XM_005271327.2:c.920A=	XP_005271384.1:p.Lys307=
XM_005271322.4:c.1337A=	XP_005271379.1:p.Lys446=
XM_005271323.4:c.1295A=	XP_005271380.1:p.Lys432=
XM_005271324.5:c.1145A=	XP_005271381.1:p.Lys382=
XM_005271325.4:c.1251+2429A=	XP_005271382.1:n.1251+2429A=
XM_005271326.4:c.1103A=	XP_005271383.1:p.Lys368=
XM_005271327.4:c.920A=	XP_005271384.1:p.Lys307=
NM_001172309.2:c.1145A=	NP_001165780.1:p.Lys382=
NM_144573.4:c.1337A= MANE Select	NP_653174.3:p.Lys446=