Canonical Allele Identifier: CA2574166357

Gene: NEXN

Linked Data

• gnomAD v4: 1-77942989-CA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942995del , CM000663.2:g.77942995del	GRCh38
NC_000001.10:g.78408680del , CM000663.1:g.78408680del	GRCh37
NC_000001.9:g.78181268del	NCBI36
NG_016625.1:g.59481del , LRG_442:g.59481del
NG_033243.2:g.41104del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.*166del MANE Select	ENSP00000333938.7:n.*166del
ENST00000330010.12:c.*166del	ENSP00000327363.8:n.*166del
ENST00000334785.11:c.*166del	ENSP00000333938.7:n.*166del
ENST00000342754.5:c.1812del
ENST00000480732.2:n.1768del
NM_001172309.1:c.*166del	NP_001165780.1:n.*166del
NM_144573.3:c.*166del , LRG_442t1:c.*166del	NP_653174.3:n.*166del
XM_005271322.2:c.*82del	XP_005271379.1:n.*82del
XM_005271323.2:c.*82del	XP_005271380.1:n.*82del
XM_005271324.3:c.*82del	XP_005271381.1:n.*82del
XM_005271325.2:c.*82del	XP_005271382.1:n.*82del
XM_005271326.2:c.*82del	XP_005271383.1:n.*82del
XM_005271327.2:c.*82del	XP_005271384.1:n.*82del
XM_005271322.4:c.*82del	XP_005271379.1:n.*82del
XM_005271323.4:c.*82del	XP_005271380.1:n.*82del
XM_005271324.5:c.*82del	XP_005271381.1:n.*82del
XM_005271325.4:c.*82del	XP_005271382.1:n.*82del
XM_005271326.4:c.*82del	XP_005271383.1:n.*82del
XM_005271327.4:c.*82del	XP_005271384.1:n.*82del
NM_001172309.2:c.*166del	NP_001165780.1:n.*166del
NM_144573.4:c.*166del MANE Select	NP_653174.3:n.*166del