Canonical Allele Identifier: CA1146281875

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77943042C= , CM000663.2:g.77943042C=	GRCh38
NC_000001.10:g.78408727C= , CM000663.1:g.78408727C=	GRCh37
NC_000001.9:g.78181315C=	NCBI36
NG_016625.1:g.59528C= , LRG_442:g.59528C=
NG_033243.2:g.41052G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.*213C= MANE Select	ENSP00000333938.7:n.*213C=
ENST00000330010.12:c.*213C=	ENSP00000327363.8:n.*213C=
ENST00000334785.11:c.*213C=	ENSP00000333938.7:n.*213C=
ENST00000342754.5:c.1859C=
ENST00000480732.2:n.1815C=
NM_001172309.1:c.*213C=	NP_001165780.1:n.*213C=
NM_144573.3:c.*213C= , LRG_442t1:c.*213C=	NP_653174.3:n.*213C=
XM_005271322.2:c.*129C=	XP_005271379.1:n.*129C=
XM_005271323.2:c.*129C=	XP_005271380.1:n.*129C=
XM_005271324.3:c.*129C=	XP_005271381.1:n.*129C=
XM_005271325.2:c.*129C=	XP_005271382.1:n.*129C=
XM_005271326.2:c.*129C=	XP_005271383.1:n.*129C=
XM_005271327.2:c.*129C=	XP_005271384.1:n.*129C=
XM_005271322.4:c.*129C=	XP_005271379.1:n.*129C=
XM_005271323.4:c.*129C=	XP_005271380.1:n.*129C=
XM_005271324.5:c.*129C=	XP_005271381.1:n.*129C=
XM_005271325.4:c.*129C=	XP_005271382.1:n.*129C=
XM_005271326.4:c.*129C=	XP_005271383.1:n.*129C=
XM_005271327.4:c.*129C=	XP_005271384.1:n.*129C=
NM_001172309.2:c.*213C=	NP_001165780.1:n.*213C=
NM_144573.4:c.*213C= MANE Select	NP_653174.3:n.*213C=