Canonical Allele Identifier: CA418709230

Gene: NEXN

Linked Data

• MyVariant Identifiers: chr1:g.78383886A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77918201A>T , CM000663.2:g.77918201A>T	GRCh38
NC_000001.10:g.78383886A>T , CM000663.1:g.78383886A>T	GRCh37
NC_000001.9:g.78156474A>T	NCBI36
NG_016625.1:g.34687A>T , LRG_442:g.34687A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000334785.12:c.375A>T MANE Select	ENSP00000333938.7:p.Arg125=
ENST00000330010.12:c.183A>T	ENSP00000327363.8:p.Arg61=
ENST00000334785.11:c.375A>T	ENSP00000333938.7:p.Arg125=
ENST00000342754.5:c.74A>T
ENST00000401035.7:c.183A>T	ENSP00000383814.3:p.Arg61=
ENST00000440324.5:c.375A>T	ENSP00000411902.1:p.Arg125=
NM_001172309.1:c.183A>T	NP_001165780.1:p.Arg61=
NM_144573.3:c.375A>T , LRG_442t1:c.375A>T	NP_653174.3:p.Arg125=
XM_005271322.2:c.375A>T	XP_005271379.1:p.Arg125=
XM_005271323.2:c.375A>T	XP_005271380.1:p.Arg125=
XM_005271324.3:c.183A>T	XP_005271381.1:p.Arg61=
XM_005271325.2:c.375A>T	XP_005271382.1:p.Arg125=
XM_005271326.2:c.183A>T	XP_005271383.1:p.Arg61=
XM_005271327.2:c.375A>T	XP_005271384.1:p.Arg125=
XM_005271322.4:c.375A>T	XP_005271379.1:p.Arg125=
XM_005271323.4:c.375A>T	XP_005271380.1:p.Arg125=
XM_005271324.5:c.183A>T	XP_005271381.1:p.Arg61=
XM_005271325.4:c.375A>T	XP_005271382.1:p.Arg125=
XM_005271326.4:c.183A>T	XP_005271383.1:p.Arg61=
XM_005271327.4:c.375A>T	XP_005271384.1:p.Arg125=
NM_001172309.2:c.183A>T	NP_001165780.1:p.Arg61=
NM_144573.4:c.375A>T MANE Select	NP_653174.3:p.Arg125=