Canonical Allele Identifier: CA1177628298

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77935913C= , CM000663.2:g.77935913C=	GRCh38
NC_000001.10:g.78401598C= , CM000663.1:g.78401598C=	GRCh37
NC_000001.9:g.78174186C=	NCBI36
NG_016625.1:g.52399C= , LRG_442:g.52399C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1342C= MANE Select	ENSP00000333938.7:p.Leu448=
ENST00000330010.12:c.1150C=	ENSP00000327363.8:p.Leu384=
ENST00000334785.11:c.1342C=	ENSP00000333938.7:p.Leu448=
ENST00000342754.5:c.1041C=
ENST00000440324.5:c.1300C=	ENSP00000411902.1:p.Leu434=
ENST00000464998.1:n.802C=
ENST00000480732.2:n.916C=
NM_001172309.1:c.1150C=	NP_001165780.1:p.Leu384=
NM_144573.3:c.1342C= , LRG_442t1:c.1342C=	NP_653174.3:p.Leu448=
XM_005271322.2:c.1342C=	XP_005271379.1:p.Leu448=
XM_005271323.2:c.1300C=	XP_005271380.1:p.Leu434=
XM_005271324.3:c.1150C=	XP_005271381.1:p.Leu384=
XM_005271325.2:c.1251+2434C=	XP_005271382.1:n.1251+2434C=
XM_005271326.2:c.1108C=	XP_005271383.1:p.Leu370=
XM_005271327.2:c.925C=	XP_005271384.1:p.Leu309=
XM_005271322.4:c.1342C=	XP_005271379.1:p.Leu448=
XM_005271323.4:c.1300C=	XP_005271380.1:p.Leu434=
XM_005271324.5:c.1150C=	XP_005271381.1:p.Leu384=
XM_005271325.4:c.1251+2434C=	XP_005271382.1:n.1251+2434C=
XM_005271326.4:c.1108C=	XP_005271383.1:p.Leu370=
XM_005271327.4:c.925C=	XP_005271384.1:p.Leu309=
NM_001172309.2:c.1150C=	NP_001165780.1:p.Leu384=
NM_144573.4:c.1342C= MANE Select	NP_653174.3:p.Leu448=