Canonical Allele Identifier: CA1147942336

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942213C= , CM000663.2:g.77942213C=	GRCh38
NC_000001.10:g.78407898C= , CM000663.1:g.78407898C=	GRCh37
NC_000001.9:g.78180486C=	NCBI36
NG_016625.1:g.58699C= , LRG_442:g.58699C=
NG_033243.2:g.41881G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000334785.12:c.1659+5C= MANE Select	ENSP00000333938.7:n.1659+5C=
ENST00000330010.12:c.1467+5C=	ENSP00000327363.8:n.1467+5C=
ENST00000334785.11:c.1659+5C=	ENSP00000333938.7:n.1659+5C=
ENST00000342754.5:c.1358+5C=
ENST00000470735.1:n.498+5C=
ENST00000480732.2:n.1233+5C=
NM_001172309.1:c.1467+5C=	NP_001165780.1:n.1467+5C=
NM_144573.3:c.1659+5C= , LRG_442t1:c.1659+5C=	NP_653174.3:n.1659+5C=
XM_005271322.2:c.1659+5C=	XP_005271379.1:n.1659+5C=
XM_005271323.2:c.1617+5C=	XP_005271380.1:n.1617+5C=
XM_005271324.3:c.1467+5C=	XP_005271381.1:n.1467+5C=
XM_005271325.2:c.1437+5C=	XP_005271382.1:n.1437+5C=
XM_005271326.2:c.1425+5C=	XP_005271383.1:n.1425+5C=
XM_005271327.2:c.1242+5C=	XP_005271384.1:n.1242+5C=
XM_005271322.4:c.1659+5C=	XP_005271379.1:n.1659+5C=
XM_005271323.4:c.1617+5C=	XP_005271380.1:n.1617+5C=
XM_005271324.5:c.1467+5C=	XP_005271381.1:n.1467+5C=
XM_005271325.4:c.1437+5C=	XP_005271382.1:n.1437+5C=
XM_005271326.4:c.1425+5C=	XP_005271383.1:n.1425+5C=
XM_005271327.4:c.1242+5C=	XP_005271384.1:n.1242+5C=
NM_001172309.2:c.1467+5C=	NP_001165780.1:n.1467+5C=
NM_144573.4:c.1659+5C= MANE Select	NP_653174.3:n.1659+5C=