Canonical Allele Identifier: CA2646301315

Gene: NEXN

Linked Data

• gnomAD v4: 1-77943081-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77943085del , CM000663.2:g.77943085del	GRCh38
NC_000001.10:g.78408770del , CM000663.1:g.78408770del	GRCh37
NC_000001.9:g.78181358del	NCBI36
NG_016625.1:g.59571del , LRG_442:g.59571del
NG_033243.2:g.41012del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.*256del MANE Select	ENSP00000333938.7:n.*256del
ENST00000330010.12:c.*256del	ENSP00000327363.8:n.*256del
ENST00000334785.11:c.*256del	ENSP00000333938.7:n.*256del
ENST00000342754.5:c.1902del
ENST00000480732.2:n.1858del
NM_001172309.1:c.*256del	NP_001165780.1:n.*256del
NM_144573.3:c.*256del , LRG_442t1:c.*256del	NP_653174.3:n.*256del
XM_005271322.2:c.*172del	XP_005271379.1:n.*172del
XM_005271323.2:c.*172del	XP_005271380.1:n.*172del
XM_005271324.3:c.*172del	XP_005271381.1:n.*172del
XM_005271325.2:c.*172del	XP_005271382.1:n.*172del
XM_005271326.2:c.*172del	XP_005271383.1:n.*172del
XM_005271327.2:c.*172del	XP_005271384.1:n.*172del
XM_005271322.4:c.*172del	XP_005271379.1:n.*172del
XM_005271323.4:c.*172del	XP_005271380.1:n.*172del
XM_005271324.5:c.*172del	XP_005271381.1:n.*172del
XM_005271325.4:c.*172del	XP_005271382.1:n.*172del
XM_005271326.4:c.*172del	XP_005271383.1:n.*172del
XM_005271327.4:c.*172del	XP_005271384.1:n.*172del
NM_001172309.2:c.*256del	NP_001165780.1:n.*256del
NM_144573.4:c.*256del MANE Select	NP_653174.3:n.*256del