Canonical Allele Identifier: CA1147623050

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77917605G= , CM000663.2:g.77917605G=	GRCh38
NC_000001.10:g.78383290G= , CM000663.1:g.78383290G=	GRCh37
NC_000001.9:g.78155878G=	NCBI36
NG_016625.1:g.34091G= , LRG_442:g.34091G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.67G= MANE Select	ENSP00000333938.7:p.Val23=
ENST00000330010.12:c.28-355G=	ENSP00000327363.8:n.28-355G=
ENST00000334785.11:c.67G=	ENSP00000333938.7:p.Val23=
ENST00000401035.7:c.28-355G=	ENSP00000383814.3:n.28-355G=
ENST00000440324.5:c.67G=	ENSP00000411902.1:p.Val23=
NM_001172309.1:c.28-355G=	NP_001165780.1:n.28-355G=
NM_144573.3:c.67G= , LRG_442t1:c.67G=	NP_653174.3:p.Val23=
XM_005271322.2:c.67G=	XP_005271379.1:p.Val23=
XM_005271323.2:c.67G=	XP_005271380.1:p.Val23=
XM_005271324.3:c.28-355G=	XP_005271381.1:n.28-355G=
XM_005271325.2:c.67G=	XP_005271382.1:p.Val23=
XM_005271326.2:c.28-355G=	XP_005271383.1:n.28-355G=
XM_005271327.2:c.67G=	XP_005271384.1:p.Val23=
XM_005271322.4:c.67G=	XP_005271379.1:p.Val23=
XM_005271323.4:c.67G=	XP_005271380.1:p.Val23=
XM_005271324.5:c.28-355G=	XP_005271381.1:n.28-355G=
XM_005271325.4:c.67G=	XP_005271382.1:p.Val23=
XM_005271326.4:c.28-355G=	XP_005271383.1:n.28-355G=
XM_005271327.4:c.67G=	XP_005271384.1:p.Val23=
NM_001172309.2:c.28-355G=	NP_001165780.1:n.28-355G=
NM_144573.4:c.67G= MANE Select	NP_653174.3:p.Val23=