Canonical Allele Identifier: CA2646274711

Gene: NEXN

Linked Data

• gnomAD v4: 1-77935823-GA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77935825del , CM000663.2:g.77935825del	GRCh38
NC_000001.10:g.78401510del , CM000663.1:g.78401510del	GRCh37
NC_000001.9:g.78174098del	NCBI36
NG_016625.1:g.52311del , LRG_442:g.52311del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1254del MANE Select	ENSP00000333938.7:p.Glu419ArgfsTer9
ENST00000330010.12:c.1062del	ENSP00000327363.8:p.Glu355ArgfsTer9
ENST00000334785.11:c.1254del	ENSP00000333938.7:p.Glu419ArgfsTer9
ENST00000342754.5:c.953del
ENST00000440324.5:c.1212del	ENSP00000411902.1:p.Glu405ArgfsTer9
ENST00000464998.1:n.714del
ENST00000480732.2:n.828del
NM_001172309.1:c.1062del	NP_001165780.1:p.Glu355ArgfsTer9
NM_144573.3:c.1254del , LRG_442t1:c.1254del	NP_653174.3:p.Glu419ArgfsTer9
XM_005271322.2:c.1254del	XP_005271379.1:p.Glu419ArgfsTer9
XM_005271323.2:c.1212del	XP_005271380.1:p.Glu405ArgfsTer9
XM_005271324.3:c.1062del	XP_005271381.1:p.Glu355ArgfsTer9
XM_005271325.2:c.1251+2346del	XP_005271382.1:n.1251+2346del
XM_005271326.2:c.1020del	XP_005271383.1:p.Glu341ArgfsTer9
XM_005271327.2:c.837del	XP_005271384.1:p.Glu280ArgfsTer9
XM_005271322.4:c.1254del	XP_005271379.1:p.Glu419ArgfsTer9
XM_005271323.4:c.1212del	XP_005271380.1:p.Glu405ArgfsTer9
XM_005271324.5:c.1062del	XP_005271381.1:p.Glu355ArgfsTer9
XM_005271325.4:c.1251+2346del	XP_005271382.1:n.1251+2346del
XM_005271326.4:c.1020del	XP_005271383.1:p.Glu341ArgfsTer9
XM_005271327.4:c.837del	XP_005271384.1:p.Glu280ArgfsTer9
NM_001172309.2:c.1062del	NP_001165780.1:p.Glu355ArgfsTer9
NM_144573.4:c.1254del MANE Select	NP_653174.3:p.Glu419ArgfsTer9