Canonical Allele Identifier: CA340886895

Gene: NEXN

Linked Data

• MyVariant Identifiers: chr1:g.78383894G>T (hg19) ; chr1:g.77918209G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77918209G>T , CM000663.2:g.77918209G>T	GRCh38
NC_000001.10:g.78383894G>T , CM000663.1:g.78383894G>T	GRCh37
NC_000001.9:g.78156482G>T	NCBI36
NG_016625.1:g.34695G>T , LRG_442:g.34695G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.383G>T MANE Select	ENSP00000333938.7:p.Arg128Ile
ENST00000330010.12:c.191G>T	ENSP00000327363.8:p.Arg64Ile
ENST00000334785.11:c.383G>T	ENSP00000333938.7:p.Arg128Ile
ENST00000342754.5:c.82G>T
ENST00000401035.7:c.191G>T	ENSP00000383814.3:p.Arg64Ile
ENST00000440324.5:c.383G>T	ENSP00000411902.1:p.Arg128Ile
NM_001172309.1:c.191G>T	NP_001165780.1:p.Arg64Ile
NM_144573.3:c.383G>T , LRG_442t1:c.383G>T	NP_653174.3:p.Arg128Ile
XM_005271322.2:c.383G>T	XP_005271379.1:p.Arg128Ile
XM_005271323.2:c.383G>T	XP_005271380.1:p.Arg128Ile
XM_005271324.3:c.191G>T	XP_005271381.1:p.Arg64Ile
XM_005271325.2:c.383G>T	XP_005271382.1:p.Arg128Ile
XM_005271326.2:c.191G>T	XP_005271383.1:p.Arg64Ile
XM_005271327.2:c.383G>T	XP_005271384.1:p.Arg128Ile
XM_005271322.4:c.383G>T	XP_005271379.1:p.Arg128Ile
XM_005271323.4:c.383G>T	XP_005271380.1:p.Arg128Ile
XM_005271324.5:c.191G>T	XP_005271381.1:p.Arg64Ile
XM_005271325.4:c.383G>T	XP_005271382.1:p.Arg128Ile
XM_005271326.4:c.191G>T	XP_005271383.1:p.Arg64Ile
XM_005271327.4:c.383G>T	XP_005271384.1:p.Arg128Ile
NM_001172309.2:c.191G>T	NP_001165780.1:p.Arg64Ile
NM_144573.4:c.383G>T MANE Select	NP_653174.3:p.Arg128Ile