Canonical Allele Identifier: CA1177626379

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942931T= , CM000663.2:g.77942931T=	GRCh38
NC_000001.10:g.78408616T= , CM000663.1:g.78408616T=	GRCh37
NC_000001.9:g.78181204T=	NCBI36
NG_016625.1:g.59417T= , LRG_442:g.59417T=
NG_033243.2:g.41163A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.*102T= MANE Select	ENSP00000333938.7:n.*102T=
ENST00000330010.12:c.*102T=	ENSP00000327363.8:n.*102T=
ENST00000334785.11:c.*102T=	ENSP00000333938.7:n.*102T=
ENST00000342754.5:c.1748T=
ENST00000480732.2:n.1704T=
NM_001172309.1:c.*102T=	NP_001165780.1:n.*102T=
NM_144573.3:c.*102T= , LRG_442t1:c.*102T=	NP_653174.3:n.*102T=
XM_005271322.2:c.*18T=	XP_005271379.1:n.*18T=
XM_005271323.2:c.*18T=	XP_005271380.1:n.*18T=
XM_005271324.3:c.*18T=	XP_005271381.1:n.*18T=
XM_005271325.2:c.*18T=	XP_005271382.1:n.*18T=
XM_005271326.2:c.*18T=	XP_005271383.1:n.*18T=
XM_005271327.2:c.*18T=	XP_005271384.1:n.*18T=
XM_005271322.4:c.*18T=	XP_005271379.1:n.*18T=
XM_005271323.4:c.*18T=	XP_005271380.1:n.*18T=
XM_005271324.5:c.*18T=	XP_005271381.1:n.*18T=
XM_005271325.4:c.*18T=	XP_005271382.1:n.*18T=
XM_005271326.4:c.*18T=	XP_005271383.1:n.*18T=
XM_005271327.4:c.*18T=	XP_005271384.1:n.*18T=
NM_001172309.2:c.*102T=	NP_001165780.1:n.*102T=
NM_144573.4:c.*102T= MANE Select	NP_653174.3:n.*102T=