Canonical Allele Identifier: CA1177631107

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77941987G= , CM000663.2:g.77941987G=	GRCh38
NC_000001.10:g.78407672G= , CM000663.1:g.78407672G=	GRCh37
NC_000001.9:g.78180260G=	NCBI36
NG_016625.1:g.58473G= , LRG_442:g.58473G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000334785.12:c.1474-36G= MANE Select	ENSP00000333938.7:n.1474-36G=
ENST00000330010.12:c.1282-36G=	ENSP00000327363.8:n.1282-36G=
ENST00000334785.11:c.1474-36G=	ENSP00000333938.7:n.1474-36G=
ENST00000342754.5:c.1173-36G=
ENST00000470735.1:n.277G=
ENST00000480732.2:n.1048-36G=
NM_001172309.1:c.1282-36G=	NP_001165780.1:n.1282-36G=
NM_144573.3:c.1474-36G= , LRG_442t1:c.1474-36G=	NP_653174.3:n.1474-36G=
XM_005271322.2:c.1474-36G=	XP_005271379.1:n.1474-36G=
XM_005271323.2:c.1432-36G=	XP_005271380.1:n.1432-36G=
XM_005271324.3:c.1282-36G=	XP_005271381.1:n.1282-36G=
XM_005271325.2:c.1252-36G=	XP_005271382.1:n.1252-36G=
XM_005271326.2:c.1240-36G=	XP_005271383.1:n.1240-36G=
XM_005271327.2:c.1057-36G=	XP_005271384.1:n.1057-36G=
XM_005271322.4:c.1474-36G=	XP_005271379.1:n.1474-36G=
XM_005271323.4:c.1432-36G=	XP_005271380.1:n.1432-36G=
XM_005271324.5:c.1282-36G=	XP_005271381.1:n.1282-36G=
XM_005271325.4:c.1252-36G=	XP_005271382.1:n.1252-36G=
XM_005271326.4:c.1240-36G=	XP_005271383.1:n.1240-36G=
XM_005271327.4:c.1057-36G=	XP_005271384.1:n.1057-36G=
NM_001172309.2:c.1282-36G=	NP_001165780.1:n.1282-36G=
NM_144573.4:c.1474-36G= MANE Select	NP_653174.3:n.1474-36G=