Canonical Allele Identifier: CA2580063261

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942731del , CM000663.2:g.77942731del	GRCh38
NC_000001.10:g.78408416del , CM000663.1:g.78408416del	GRCh37
NC_000001.9:g.78181004del	NCBI36
NG_016625.1:g.59217del , LRG_442:g.59217del
NG_033243.2:g.41365del

Transcript Alleles

HGVS	Amino-acid Change
NM_144573.4:c.1930del MANE Select	NP_653174.3:p.Thr644LeufsTer?
ENST00000334785.12:c.1930del MANE Select	ENSP00000333938.7:p.Thr644LeufsTer?
NM_001172309.1:c.1738del	NP_001165780.1:p.Thr580LeufsTer?
NM_001172309.2:c.1738del	NP_001165780.1:p.Thr580LeufsTer?
NM_144573.3:c.1930del , LRG_442t1:c.1930del	NP_653174.3:p.Thr644LeufsTer?
ENST00000330010.12:c.1738del	ENSP00000327363.8:p.Thr580LeufsTer?
ENST00000334785.11:c.1930del	ENSP00000333938.7:p.Thr644LeufsTer?
ENST00000342754.5:c.1629del
ENST00000470735.1:n.769del
ENST00000480732.2:n.1504del
XM_005271322.2:c.1930del	XP_005271379.1:p.Thr644LeufsTer?
XM_005271322.4:c.1930del	XP_005271379.1:p.Thr644LeufsTer?
XM_005271323.2:c.1888del	XP_005271380.1:p.Thr630LeufsTer?
XM_005271323.4:c.1888del	XP_005271380.1:p.Thr630LeufsTer?
XM_005271324.3:c.1738del	XP_005271381.1:p.Thr580LeufsTer?
XM_005271324.5:c.1738del	XP_005271381.1:p.Thr580LeufsTer?
XM_005271325.2:c.1708del	XP_005271382.1:p.Thr570LeufsTer?
XM_005271325.4:c.1708del	XP_005271382.1:p.Thr570LeufsTer?
XM_005271326.2:c.1696del	XP_005271383.1:p.Thr566LeufsTer?
XM_005271326.4:c.1696del	XP_005271383.1:p.Thr566LeufsTer?
XM_005271327.2:c.1513del	XP_005271384.1:p.Thr505LeufsTer?
XM_005271327.4:c.1513del	XP_005271384.1:p.Thr505LeufsTer?