Canonical Allele Identifier: CA2646301168

Gene: NEXN

Linked Data

• gnomAD v4: 1-77917501-ATCTTT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77917502_77917506del , CM000663.2:g.77917502_77917506del	GRCh38
NC_000001.10:g.78383187_78383191del , CM000663.1:g.78383187_78383191del	GRCh37
NC_000001.9:g.78155775_78155779del	NCBI36
NG_016625.1:g.33988_33992del , LRG_442:g.33988_33992del

Transcript Alleles

HGVS	Amino-acid change
ENST00000334785.12:c.28-64_28-60del MANE Select	ENSP00000333938.7:n.28-64_28-60del
ENST00000330010.12:c.28-458_28-454del	ENSP00000327363.8:n.28-458_28-454del
ENST00000334785.11:c.28-64_28-60del	ENSP00000333938.7:n.28-64_28-60del
ENST00000401035.7:c.28-458_28-454del	ENSP00000383814.3:n.28-458_28-454del
ENST00000440324.5:c.28-64_28-60del	ENSP00000411902.1:n.28-64_28-60del
NM_001172309.1:c.28-458_28-454del	NP_001165780.1:n.28-458_28-454del
NM_144573.3:c.28-64_28-60del , LRG_442t1:c.28-64_28-60del	NP_653174.3:n.28-64_28-60del
XM_005271322.2:c.28-64_28-60del	XP_005271379.1:n.28-64_28-60del
XM_005271323.2:c.28-64_28-60del	XP_005271380.1:n.28-64_28-60del
XM_005271324.3:c.28-458_28-454del	XP_005271381.1:n.28-458_28-454del
XM_005271325.2:c.28-64_28-60del	XP_005271382.1:n.28-64_28-60del
XM_005271326.2:c.28-458_28-454del	XP_005271383.1:n.28-458_28-454del
XM_005271327.2:c.28-64_28-60del	XP_005271384.1:n.28-64_28-60del
XM_005271322.4:c.28-64_28-60del	XP_005271379.1:n.28-64_28-60del
XM_005271323.4:c.28-64_28-60del	XP_005271380.1:n.28-64_28-60del
XM_005271324.5:c.28-458_28-454del	XP_005271381.1:n.28-458_28-454del
XM_005271325.4:c.28-64_28-60del	XP_005271382.1:n.28-64_28-60del
XM_005271326.4:c.28-458_28-454del	XP_005271383.1:n.28-458_28-454del
XM_005271327.4:c.28-64_28-60del	XP_005271384.1:n.28-64_28-60del
NM_001172309.2:c.28-458_28-454del	NP_001165780.1:n.28-458_28-454del
NM_144573.4:c.28-64_28-60del MANE Select	NP_653174.3:n.28-64_28-60del