Canonical Allele Identifier: CA523842816

Gene: NEXN

Linked Data

• dbSNP Id: rs1315424903
• gnomAD v2: 1-78408591-AC-A
• gnomAD v4: 1-77942906-AC-A
• MyVariant Identifiers: chr1:g.78408592del (hg19) ; chr1:g.77942907del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942907del , CM000663.2:g.77942907del	GRCh38
NC_000001.10:g.78408592del , CM000663.1:g.78408592del	GRCh37
NC_000001.9:g.78181180del	NCBI36
NG_016625.1:g.59393del , LRG_442:g.59393del
NG_033243.2:g.41187del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.*78del MANE Select	ENSP00000333938.7:n.*78del
ENST00000330010.12:c.*78del	ENSP00000327363.8:n.*78del
ENST00000334785.11:c.*78del	ENSP00000333938.7:n.*78del
ENST00000342754.5:c.1724del
ENST00000480732.2:n.1680del
NM_001172309.1:c.*78del	NP_001165780.1:n.*78del
NM_144573.3:c.*78del , LRG_442t1:c.*78del	NP_653174.3:n.*78del
XM_005271322.2:c.2025del	XP_005271379.1:p.Tyr676ThrfsTer?
XM_005271323.2:c.1983del	XP_005271380.1:p.Tyr662ThrfsTer?
XM_005271324.3:c.1833del	XP_005271381.1:p.Tyr612ThrfsTer?
XM_005271325.2:c.1803del	XP_005271382.1:p.Tyr602ThrfsTer?
XM_005271326.2:c.1791del	XP_005271383.1:p.Tyr598ThrfsTer?
XM_005271327.2:c.1608del	XP_005271384.1:p.Tyr537ThrfsTer?
XM_005271322.4:c.2025del	XP_005271379.1:p.Tyr676ThrfsTer?
XM_005271323.4:c.1983del	XP_005271380.1:p.Tyr662ThrfsTer?
XM_005271324.5:c.1833del	XP_005271381.1:p.Tyr612ThrfsTer?
XM_005271325.4:c.1803del	XP_005271382.1:p.Tyr602ThrfsTer?
XM_005271326.4:c.1791del	XP_005271383.1:p.Tyr598ThrfsTer?
XM_005271327.4:c.1608del	XP_005271384.1:p.Tyr537ThrfsTer?
NM_001172309.2:c.*78del	NP_001165780.1:n.*78del
NM_144573.4:c.*78del MANE Select	NP_653174.3:n.*78del