Canonical Allele Identifier: CA739060057

Gene: NEXN

Linked Data

• dbSNP Id: rs1426239109
• gnomAD v4: 1-77942935-ACTTTCT-A
• MyVariant Identifiers: chr1:g.78408621_78408626del (hg19) ; chr1:g.77942936_77942941del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942941_77942946del , CM000663.2:g.77942941_77942946del	GRCh38
NC_000001.10:g.78408626_78408631del , CM000663.1:g.78408626_78408631del	GRCh37
NC_000001.9:g.78181214_78181219del	NCBI36
NG_016625.1:g.59427_59432del , LRG_442:g.59427_59432del
NG_033243.2:g.41153_41158del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.*112_*117del MANE Select	ENSP00000333938.7:n.*112_*117del
ENST00000330010.12:c.*112_*117del	ENSP00000327363.8:n.*112_*117del
ENST00000334785.11:c.*112_*117del	ENSP00000333938.7:n.*112_*117del
ENST00000342754.5:c.1758_1763del
ENST00000480732.2:n.1714_1719del
NM_001172309.1:c.*112_*117del	NP_001165780.1:n.*112_*117del
NM_144573.3:c.*112_*117del , LRG_442t1:c.*112_*117del	NP_653174.3:n.*112_*117del
XM_005271322.2:c.*28_*33del	XP_005271379.1:n.*28_*33del
XM_005271323.2:c.*28_*33del	XP_005271380.1:n.*28_*33del
XM_005271324.3:c.*28_*33del	XP_005271381.1:n.*28_*33del
XM_005271325.2:c.*28_*33del	XP_005271382.1:n.*28_*33del
XM_005271326.2:c.*28_*33del	XP_005271383.1:n.*28_*33del
XM_005271327.2:c.*28_*33del	XP_005271384.1:n.*28_*33del
XM_005271322.4:c.*28_*33del	XP_005271379.1:n.*28_*33del
XM_005271323.4:c.*28_*33del	XP_005271380.1:n.*28_*33del
XM_005271324.5:c.*28_*33del	XP_005271381.1:n.*28_*33del
XM_005271325.4:c.*28_*33del	XP_005271382.1:n.*28_*33del
XM_005271326.4:c.*28_*33del	XP_005271383.1:n.*28_*33del
XM_005271327.4:c.*28_*33del	XP_005271384.1:n.*28_*33del
NM_001172309.2:c.*112_*117del	NP_001165780.1:n.*112_*117del
NM_144573.4:c.*112_*117del MANE Select	NP_653174.3:n.*112_*117del