Canonical Allele Identifier: CA1177620320

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77918132G= , CM000663.2:g.77918132G=	GRCh38
NC_000001.10:g.78383817G= , CM000663.1:g.78383817G=	GRCh37
NC_000001.9:g.78156405G=	NCBI36
NG_016625.1:g.34618G= , LRG_442:g.34618G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.306G= MANE Select	ENSP00000333938.7:p.Val102=
ENST00000330010.12:c.114G=	ENSP00000327363.8:p.Val38=
ENST00000334785.11:c.306G=	ENSP00000333938.7:p.Val102=
ENST00000342754.5:c.5G=
ENST00000401035.7:c.114G=	ENSP00000383814.3:p.Val38=
ENST00000440324.5:c.306G=	ENSP00000411902.1:p.Val102=
NM_001172309.1:c.114G=	NP_001165780.1:p.Val38=
NM_144573.3:c.306G= , LRG_442t1:c.306G=	NP_653174.3:p.Val102=
XM_005271322.2:c.306G=	XP_005271379.1:p.Val102=
XM_005271323.2:c.306G=	XP_005271380.1:p.Val102=
XM_005271324.3:c.114G=	XP_005271381.1:p.Val38=
XM_005271325.2:c.306G=	XP_005271382.1:p.Val102=
XM_005271326.2:c.114G=	XP_005271383.1:p.Val38=
XM_005271327.2:c.306G=	XP_005271384.1:p.Val102=
XM_005271322.4:c.306G=	XP_005271379.1:p.Val102=
XM_005271323.4:c.306G=	XP_005271380.1:p.Val102=
XM_005271324.5:c.114G=	XP_005271381.1:p.Val38=
XM_005271325.4:c.306G=	XP_005271382.1:p.Val102=
XM_005271326.4:c.114G=	XP_005271383.1:p.Val38=
XM_005271327.4:c.306G=	XP_005271384.1:p.Val102=
NM_001172309.2:c.114G=	NP_001165780.1:p.Val38=
NM_144573.4:c.306G= MANE Select	NP_653174.3:p.Val102=