Canonical Allele Identifier: CA1177628440

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77936217C= , CM000663.2:g.77936217C=	GRCh38
NC_000001.10:g.78401902C= , CM000663.1:g.78401902C=	GRCh37
NC_000001.9:g.78174490C=	NCBI36
NG_016625.1:g.52703C= , LRG_442:g.52703C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1473+173C= MANE Select	ENSP00000333938.7:n.1473+173C=
ENST00000330010.12:c.1281+173C=	ENSP00000327363.8:n.1281+173C=
ENST00000334785.11:c.1473+173C=	ENSP00000333938.7:n.1473+173C=
ENST00000342754.5:c.1172+173C=
ENST00000480732.2:n.1047+173C=
NM_001172309.1:c.1281+173C=	NP_001165780.1:n.1281+173C=
NM_144573.3:c.1473+173C= , LRG_442t1:c.1473+173C=	NP_653174.3:n.1473+173C=
XM_005271322.2:c.1473+173C=	XP_005271379.1:n.1473+173C=
XM_005271323.2:c.1431+173C=	XP_005271380.1:n.1431+173C=
XM_005271324.3:c.1281+173C=	XP_005271381.1:n.1281+173C=
XM_005271325.2:c.1251+2738C=	XP_005271382.1:n.1251+2738C=
XM_005271326.2:c.1239+173C=	XP_005271383.1:n.1239+173C=
XM_005271327.2:c.1056+173C=	XP_005271384.1:n.1056+173C=
XM_005271322.4:c.1473+173C=	XP_005271379.1:n.1473+173C=
XM_005271323.4:c.1431+173C=	XP_005271380.1:n.1431+173C=
XM_005271324.5:c.1281+173C=	XP_005271381.1:n.1281+173C=
XM_005271325.4:c.1251+2738C=	XP_005271382.1:n.1251+2738C=
XM_005271326.4:c.1239+173C=	XP_005271383.1:n.1239+173C=
XM_005271327.4:c.1056+173C=	XP_005271384.1:n.1056+173C=
NM_001172309.2:c.1281+173C=	NP_001165780.1:n.1281+173C=
NM_144573.4:c.1473+173C= MANE Select	NP_653174.3:n.1473+173C=