Canonical Allele Identifier: CA1177626682

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77933301C= , CM000663.2:g.77933301C=	GRCh38
NC_000001.10:g.78398986C= , CM000663.1:g.78398986C=	GRCh37
NC_000001.9:g.78171574C=	NCBI36
NG_016625.1:g.49787C= , LRG_442:g.49787C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000334785.12:c.1073C= MANE Select	ENSP00000333938.7:p.Pro358=
ENST00000330010.12:c.881C=	ENSP00000327363.8:p.Pro294=
ENST00000334785.11:c.1073C=	ENSP00000333938.7:p.Pro358=
ENST00000342754.5:c.772C=
ENST00000401035.7:c.881C=	ENSP00000383814.3:p.Pro294=
ENST00000440324.5:c.1031C=	ENSP00000411902.1:p.Pro344=
ENST00000464998.1:n.533C=
ENST00000480732.2:n.647C=
NM_001172309.1:c.881C=	NP_001165780.1:p.Pro294=
NM_144573.3:c.1073C= , LRG_442t1:c.1073C=	NP_653174.3:p.Pro358=
XM_005271322.2:c.1073C=	XP_005271379.1:p.Pro358=
XM_005271323.2:c.1031C=	XP_005271380.1:p.Pro344=
XM_005271324.3:c.881C=	XP_005271381.1:p.Pro294=
XM_005271325.2:c.1073C=	XP_005271382.1:p.Pro358=
XM_005271326.2:c.839C=	XP_005271383.1:p.Pro280=
XM_005271327.2:c.656C=	XP_005271384.1:p.Pro219=
XM_005271322.4:c.1073C=	XP_005271379.1:p.Pro358=
XM_005271323.4:c.1031C=	XP_005271380.1:p.Pro344=
XM_005271324.5:c.881C=	XP_005271381.1:p.Pro294=
XM_005271325.4:c.1073C=	XP_005271382.1:p.Pro358=
XM_005271326.4:c.839C=	XP_005271383.1:p.Pro280=
XM_005271327.4:c.656C=	XP_005271384.1:p.Pro219=
NM_001172309.2:c.881C=	NP_001165780.1:p.Pro294=
NM_144573.4:c.1073C= MANE Select	NP_653174.3:p.Pro358=