Canonical Allele Identifier: CA1177628290

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77935896C= , CM000663.2:g.77935896C=	GRCh38
NC_000001.10:g.78401581C= , CM000663.1:g.78401581C=	GRCh37
NC_000001.9:g.78174169C=	NCBI36
NG_016625.1:g.52382C= , LRG_442:g.52382C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1325C= MANE Select	ENSP00000333938.7:p.Ser442=
ENST00000330010.12:c.1133C=	ENSP00000327363.8:p.Ser378=
ENST00000334785.11:c.1325C=	ENSP00000333938.7:p.Ser442=
ENST00000342754.5:c.1024C=
ENST00000440324.5:c.1283C=	ENSP00000411902.1:p.Ser428=
ENST00000464998.1:n.785C=
ENST00000480732.2:n.899C=
NM_001172309.1:c.1133C=	NP_001165780.1:p.Ser378=
NM_144573.3:c.1325C= , LRG_442t1:c.1325C=	NP_653174.3:p.Ser442=
XM_005271322.2:c.1325C=	XP_005271379.1:p.Ser442=
XM_005271323.2:c.1283C=	XP_005271380.1:p.Ser428=
XM_005271324.3:c.1133C=	XP_005271381.1:p.Ser378=
XM_005271325.2:c.1251+2417C=	XP_005271382.1:n.1251+2417C=
XM_005271326.2:c.1091C=	XP_005271383.1:p.Ser364=
XM_005271327.2:c.908C=	XP_005271384.1:p.Ser303=
XM_005271322.4:c.1325C=	XP_005271379.1:p.Ser442=
XM_005271323.4:c.1283C=	XP_005271380.1:p.Ser428=
XM_005271324.5:c.1133C=	XP_005271381.1:p.Ser378=
XM_005271325.4:c.1251+2417C=	XP_005271382.1:n.1251+2417C=
XM_005271326.4:c.1091C=	XP_005271383.1:p.Ser364=
XM_005271327.4:c.908C=	XP_005271384.1:p.Ser303=
NM_001172309.2:c.1133C=	NP_001165780.1:p.Ser378=
NM_144573.4:c.1325C= MANE Select	NP_653174.3:p.Ser442=