Canonical Allele Identifier: CA2646274520

Gene: NEXN

Linked Data

• gnomAD v4: 1-77933367-AATT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77933372_77933374del , CM000663.2:g.77933372_77933374del	GRCh38
NC_000001.10:g.78399057_78399059del , CM000663.1:g.78399057_78399059del	GRCh37
NC_000001.9:g.78171645_78171647del	NCBI36
NG_016625.1:g.49858_49860del , LRG_442:g.49858_49860del

Transcript Alleles

HGVS	Amino-acid change
ENST00000334785.12:c.1144_1146del MANE Select	ENSP00000333938.7:p.Leu382del
ENST00000330010.12:c.952_954del	ENSP00000327363.8:p.Leu318del
ENST00000334785.11:c.1144_1146del	ENSP00000333938.7:p.Leu382del
ENST00000342754.5:c.843_845del
ENST00000401035.7:c.952_954del	ENSP00000383814.3:p.Leu318del
ENST00000440324.5:c.1102_1104del	ENSP00000411902.1:p.Leu368del
ENST00000464998.1:n.604_606del
ENST00000480732.2:n.718_720del
NM_001172309.1:c.952_954del	NP_001165780.1:p.Leu318del
NM_144573.3:c.1144_1146del , LRG_442t1:c.1144_1146del	NP_653174.3:p.Leu382del
XM_005271322.2:c.1144_1146del	XP_005271379.1:p.Leu382del
XM_005271323.2:c.1102_1104del	XP_005271380.1:p.Leu368del
XM_005271324.3:c.952_954del	XP_005271381.1:p.Leu318del
XM_005271325.2:c.1144_1146del	XP_005271382.1:p.Leu382del
XM_005271326.2:c.910_912del	XP_005271383.1:p.Leu304del
XM_005271327.2:c.727_729del	XP_005271384.1:p.Leu243del
XM_005271322.4:c.1144_1146del	XP_005271379.1:p.Leu382del
XM_005271323.4:c.1102_1104del	XP_005271380.1:p.Leu368del
XM_005271324.5:c.952_954del	XP_005271381.1:p.Leu318del
XM_005271325.4:c.1144_1146del	XP_005271382.1:p.Leu382del
XM_005271326.4:c.910_912del	XP_005271383.1:p.Leu304del
XM_005271327.4:c.727_729del	XP_005271384.1:p.Leu243del
NM_001172309.2:c.952_954del	NP_001165780.1:p.Leu318del
NM_144573.4:c.1144_1146del MANE Select	NP_653174.3:p.Leu382del