Canonical Allele Identifier: CA340878643

Gene: NEXN

Linked Data

• ClinVar Variation Id: 1502758
• ClinVar RCV Id: RCV002045249
• dbSNP Id: rs1650716200
• MyVariant Identifiers: chr1:g.78401577G>T (hg19) ; chr1:g.77935892G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77935892G>T , CM000663.2:g.77935892G>T	GRCh38
NC_000001.10:g.78401577G>T , CM000663.1:g.78401577G>T	GRCh37
NC_000001.9:g.78174165G>T	NCBI36
NG_016625.1:g.52378G>T , LRG_442:g.52378G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1321G>T MANE Select	ENSP00000333938.7:p.Gly441Cys
ENST00000330010.12:c.1129G>T	ENSP00000327363.8:p.Gly377Cys
ENST00000334785.11:c.1321G>T	ENSP00000333938.7:p.Gly441Cys
ENST00000342754.5:c.1020G>T
ENST00000440324.5:c.1279G>T	ENSP00000411902.1:p.Gly427Cys
ENST00000464998.1:n.781G>T
ENST00000480732.2:n.895G>T
NM_001172309.1:c.1129G>T	NP_001165780.1:p.Gly377Cys
NM_144573.3:c.1321G>T , LRG_442t1:c.1321G>T	NP_653174.3:p.Gly441Cys
XM_005271322.2:c.1321G>T	XP_005271379.1:p.Gly441Cys
XM_005271323.2:c.1279G>T	XP_005271380.1:p.Gly427Cys
XM_005271324.3:c.1129G>T	XP_005271381.1:p.Gly377Cys
XM_005271325.2:c.1251+2413G>T	XP_005271382.1:n.1251+2413G>T
XM_005271326.2:c.1087G>T	XP_005271383.1:p.Gly363Cys
XM_005271327.2:c.904G>T	XP_005271384.1:p.Gly302Cys
XM_005271322.4:c.1321G>T	XP_005271379.1:p.Gly441Cys
XM_005271323.4:c.1279G>T	XP_005271380.1:p.Gly427Cys
XM_005271324.5:c.1129G>T	XP_005271381.1:p.Gly377Cys
XM_005271325.4:c.1251+2413G>T	XP_005271382.1:n.1251+2413G>T
XM_005271326.4:c.1087G>T	XP_005271383.1:p.Gly363Cys
XM_005271327.4:c.904G>T	XP_005271384.1:p.Gly302Cys
NM_001172309.2:c.1129G>T	NP_001165780.1:p.Gly377Cys
NM_144573.4:c.1321G>T MANE Select	NP_653174.3:p.Gly441Cys