Canonical Allele Identifier: CA2574166246

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942002del , CM000663.2:g.77942002del	GRCh38
NC_000001.10:g.78407687del , CM000663.1:g.78407687del	GRCh37
NC_000001.9:g.78180275del	NCBI36
NG_016625.1:g.58488del , LRG_442:g.58488del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1474-21del MANE Select	ENSP00000333938.7:n.1474-21del
ENST00000330010.12:c.1282-21del	ENSP00000327363.8:n.1282-21del
ENST00000334785.11:c.1474-21del	ENSP00000333938.7:n.1474-21del
ENST00000342754.5:c.1173-21del
ENST00000470735.1:n.292del
ENST00000480732.2:n.1048-21del
NM_001172309.1:c.1282-21del	NP_001165780.1:n.1282-21del
NM_144573.3:c.1474-21del , LRG_442t1:c.1474-21del	NP_653174.3:n.1474-21del
XM_005271322.2:c.1474-21del	XP_005271379.1:n.1474-21del
XM_005271323.2:c.1432-21del	XP_005271380.1:n.1432-21del
XM_005271324.3:c.1282-21del	XP_005271381.1:n.1282-21del
XM_005271325.2:c.1252-21del	XP_005271382.1:n.1252-21del
XM_005271326.2:c.1240-21del	XP_005271383.1:n.1240-21del
XM_005271327.2:c.1057-21del	XP_005271384.1:n.1057-21del
XM_005271322.4:c.1474-21del	XP_005271379.1:n.1474-21del
XM_005271323.4:c.1432-21del	XP_005271380.1:n.1432-21del
XM_005271324.5:c.1282-21del	XP_005271381.1:n.1282-21del
XM_005271325.4:c.1252-21del	XP_005271382.1:n.1252-21del
XM_005271326.4:c.1240-21del	XP_005271383.1:n.1240-21del
XM_005271327.4:c.1057-21del	XP_005271384.1:n.1057-21del
NM_001172309.2:c.1282-21del	NP_001165780.1:n.1282-21del
NM_144573.4:c.1474-21del MANE Select	NP_653174.3:n.1474-21del