Canonical Allele Identifier: CA1177631156

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942110G= , CM000663.2:g.77942110G=	GRCh38
NC_000001.10:g.78407795G= , CM000663.1:g.78407795G=	GRCh37
NC_000001.9:g.78180383G=	NCBI36
NG_016625.1:g.58596G= , LRG_442:g.58596G=
NG_033243.2:g.41984C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1561G= MANE Select	ENSP00000333938.7:p.Ala521=
ENST00000330010.12:c.1369G=	ENSP00000327363.8:p.Ala457=
ENST00000334785.11:c.1561G=	ENSP00000333938.7:p.Ala521=
ENST00000342754.5:c.1260G=
ENST00000470735.1:n.400G=
ENST00000480732.2:n.1135G=
NM_001172309.1:c.1369G=	NP_001165780.1:p.Ala457=
NM_144573.3:c.1561G= , LRG_442t1:c.1561G=	NP_653174.3:p.Ala521=
XM_005271322.2:c.1561G=	XP_005271379.1:p.Ala521=
XM_005271323.2:c.1519G=	XP_005271380.1:p.Ala507=
XM_005271324.3:c.1369G=	XP_005271381.1:p.Ala457=
XM_005271325.2:c.1339G=	XP_005271382.1:p.Ala447=
XM_005271326.2:c.1327G=	XP_005271383.1:p.Ala443=
XM_005271327.2:c.1144G=	XP_005271384.1:p.Ala382=
XM_005271322.4:c.1561G=	XP_005271379.1:p.Ala521=
XM_005271323.4:c.1519G=	XP_005271380.1:p.Ala507=
XM_005271324.5:c.1369G=	XP_005271381.1:p.Ala457=
XM_005271325.4:c.1339G=	XP_005271382.1:p.Ala447=
XM_005271326.4:c.1327G=	XP_005271383.1:p.Ala443=
XM_005271327.4:c.1144G=	XP_005271384.1:p.Ala382=
NM_001172309.2:c.1369G=	NP_001165780.1:p.Ala457=
NM_144573.4:c.1561G= MANE Select	NP_653174.3:p.Ala521=