Canonical Allele Identifier: CA524231072

Gene: NEXN

Linked Data

• dbSNP Id: rs764505909
• gnomAD v2: 1-78407805-GAGAAGA-G
• MyVariant Identifiers: chr1:g.78407806_78407811del (hg19) ; chr1:g.77942121_77942126del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942128_77942133del , CM000663.2:g.77942128_77942133del	GRCh38
NC_000001.10:g.78407813_78407818del , CM000663.1:g.78407813_78407818del	GRCh37
NC_000001.9:g.78180401_78180406del	NCBI36
NG_016625.1:g.58614_58619del , LRG_442:g.58614_58619del
NG_033243.2:g.41968_41973del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1579_1584del MANE Select	ENSP00000333938.7:p.Glu527_Glu528del
ENST00000330010.12:c.1387_1392del	ENSP00000327363.8:p.Glu463_Glu464del
ENST00000334785.11:c.1579_1584del	ENSP00000333938.7:p.Glu527_Glu528del
ENST00000342754.5:c.1278_1283del
ENST00000470735.1:n.418_423del
ENST00000480732.2:n.1153_1158del
NM_001172309.1:c.1387_1392del	NP_001165780.1:p.Glu463_Glu464del
NM_144573.3:c.1579_1584del , LRG_442t1:c.1579_1584del	NP_653174.3:p.Glu527_Glu528del
XM_005271322.2:c.1579_1584del	XP_005271379.1:p.Glu527_Glu528del
XM_005271323.2:c.1537_1542del	XP_005271380.1:p.Glu513_Glu514del
XM_005271324.3:c.1387_1392del	XP_005271381.1:p.Glu463_Glu464del
XM_005271325.2:c.1357_1362del	XP_005271382.1:p.Glu453_Glu454del
XM_005271326.2:c.1345_1350del	XP_005271383.1:p.Glu449_Glu450del
XM_005271327.2:c.1162_1167del	XP_005271384.1:p.Glu388_Glu389del
XM_005271322.4:c.1579_1584del	XP_005271379.1:p.Glu527_Glu528del
XM_005271323.4:c.1537_1542del	XP_005271380.1:p.Glu513_Glu514del
XM_005271324.5:c.1387_1392del	XP_005271381.1:p.Glu463_Glu464del
XM_005271325.4:c.1357_1362del	XP_005271382.1:p.Glu453_Glu454del
XM_005271326.4:c.1345_1350del	XP_005271383.1:p.Glu449_Glu450del
XM_005271327.4:c.1162_1167del	XP_005271384.1:p.Glu388_Glu389del
NM_001172309.2:c.1387_1392del	NP_001165780.1:p.Glu463_Glu464del
NM_144573.4:c.1579_1584del MANE Select	NP_653174.3:p.Glu527_Glu528del