Canonical Allele Identifier: CA739060133

Gene: NEXN

Linked Data

• dbSNP Id: rs1260132765
• gnomAD v3: 1-77943091-TAAG-T
• gnomAD v4: 1-77943091-TAAG-T
• MyVariant Identifiers: chr1:g.78408777_78408779del (hg19) ; chr1:g.77943092_77943094del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77943092_77943094del , CM000663.2:g.77943092_77943094del	GRCh38
NC_000001.10:g.78408777_78408779del , CM000663.1:g.78408777_78408779del	GRCh37
NC_000001.9:g.78181365_78181367del	NCBI36
NG_016625.1:g.59578_59580del , LRG_442:g.59578_59580del
NG_033243.2:g.41000_41002del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.*263_*265del MANE Select	ENSP00000333938.7:n.*263_*265del
ENST00000330010.12:c.*263_*265del	ENSP00000327363.8:n.*263_*265del
ENST00000334785.11:c.*263_*265del	ENSP00000333938.7:n.*263_*265del
ENST00000342754.5:c.1909_1911del
ENST00000480732.2:n.1865_1867del
NM_001172309.1:c.*263_*265del	NP_001165780.1:n.*263_*265del
NM_144573.3:c.*263_*265del , LRG_442t1:c.*263_*265del	NP_653174.3:n.*263_*265del
XM_005271322.2:c.*179_*181del	XP_005271379.1:n.*179_*181del
XM_005271323.2:c.*179_*181del	XP_005271380.1:n.*179_*181del
XM_005271324.3:c.*179_*181del	XP_005271381.1:n.*179_*181del
XM_005271325.2:c.*179_*181del	XP_005271382.1:n.*179_*181del
XM_005271326.2:c.*179_*181del	XP_005271383.1:n.*179_*181del
XM_005271327.2:c.*179_*181del	XP_005271384.1:n.*179_*181del
XM_005271322.4:c.*179_*181del	XP_005271379.1:n.*179_*181del
XM_005271323.4:c.*179_*181del	XP_005271380.1:n.*179_*181del
XM_005271324.5:c.*179_*181del	XP_005271381.1:n.*179_*181del
XM_005271325.4:c.*179_*181del	XP_005271382.1:n.*179_*181del
XM_005271326.4:c.*179_*181del	XP_005271383.1:n.*179_*181del
XM_005271327.4:c.*179_*181del	XP_005271384.1:n.*179_*181del
NM_001172309.2:c.*263_*265del	NP_001165780.1:n.*263_*265del
NM_144573.4:c.*263_*265del MANE Select	NP_653174.3:n.*263_*265del