Canonical Allele Identifier: CA1177631434

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942682C= , CM000663.2:g.77942682C=	GRCh38
NC_000001.10:g.78408367C= , CM000663.1:g.78408367C=	GRCh37
NC_000001.9:g.78180955C=	NCBI36
NG_016625.1:g.59168C= , LRG_442:g.59168C=
NG_033243.2:g.41412G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1881C= MANE Select	ENSP00000333938.7:p.Asp627=
ENST00000330010.12:c.1689C=	ENSP00000327363.8:p.Asp563=
ENST00000334785.11:c.1881C=	ENSP00000333938.7:p.Asp627=
ENST00000342754.5:c.1580C=
ENST00000470735.1:n.720C=
ENST00000480732.2:n.1455C=
NM_001172309.1:c.1689C=	NP_001165780.1:p.Asp563=
NM_144573.3:c.1881C= , LRG_442t1:c.1881C=	NP_653174.3:p.Asp627=
XM_005271322.2:c.1881C=	XP_005271379.1:p.Asp627=
XM_005271323.2:c.1839C=	XP_005271380.1:p.Asp613=
XM_005271324.3:c.1689C=	XP_005271381.1:p.Asp563=
XM_005271325.2:c.1659C=	XP_005271382.1:p.Asp553=
XM_005271326.2:c.1647C=	XP_005271383.1:p.Asp549=
XM_005271327.2:c.1464C=	XP_005271384.1:p.Asp488=
XM_005271322.4:c.1881C=	XP_005271379.1:p.Asp627=
XM_005271323.4:c.1839C=	XP_005271380.1:p.Asp613=
XM_005271324.5:c.1689C=	XP_005271381.1:p.Asp563=
XM_005271325.4:c.1659C=	XP_005271382.1:p.Asp553=
XM_005271326.4:c.1647C=	XP_005271383.1:p.Asp549=
XM_005271327.4:c.1464C=	XP_005271384.1:p.Asp488=
NM_001172309.2:c.1689C=	NP_001165780.1:p.Asp563=
NM_144573.4:c.1881C= MANE Select	NP_653174.3:p.Asp627=