Canonical Allele Identifier: CA2646275334

Gene: NEXN

Linked Data

• gnomAD v4: 1-77942236-CCAAAGAT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942237_77942243del , CM000663.2:g.77942237_77942243del	GRCh38
NC_000001.10:g.78407922_78407928del , CM000663.1:g.78407922_78407928del	GRCh37
NC_000001.9:g.78180510_78180516del	NCBI36
NG_016625.1:g.58723_58729del , LRG_442:g.58723_58729del
NG_033243.2:g.41851_41857del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1659+29_1659+35del MANE Select	ENSP00000333938.7:n.1659+29_1659+35del
ENST00000330010.12:c.1467+29_1467+35del	ENSP00000327363.8:n.1467+29_1467+35del
ENST00000334785.11:c.1659+29_1659+35del	ENSP00000333938.7:n.1659+29_1659+35del
ENST00000342754.5:c.1358+29_1358+35del
ENST00000470735.1:n.498+29_498+35del
ENST00000480732.2:n.1233+29_1233+35del
NM_001172309.1:c.1467+29_1467+35del	NP_001165780.1:n.1467+29_1467+35del
NM_144573.3:c.1659+29_1659+35del , LRG_442t1:c.1659+29_1659+35del	NP_653174.3:n.1659+29_1659+35del
XM_005271322.2:c.1659+29_1659+35del	XP_005271379.1:n.1659+29_1659+35del
XM_005271323.2:c.1617+29_1617+35del	XP_005271380.1:n.1617+29_1617+35del
XM_005271324.3:c.1467+29_1467+35del	XP_005271381.1:n.1467+29_1467+35del
XM_005271325.2:c.1437+29_1437+35del	XP_005271382.1:n.1437+29_1437+35del
XM_005271326.2:c.1425+29_1425+35del	XP_005271383.1:n.1425+29_1425+35del
XM_005271327.2:c.1242+29_1242+35del	XP_005271384.1:n.1242+29_1242+35del
XM_005271322.4:c.1659+29_1659+35del	XP_005271379.1:n.1659+29_1659+35del
XM_005271323.4:c.1617+29_1617+35del	XP_005271380.1:n.1617+29_1617+35del
XM_005271324.5:c.1467+29_1467+35del	XP_005271381.1:n.1467+29_1467+35del
XM_005271325.4:c.1437+29_1437+35del	XP_005271382.1:n.1437+29_1437+35del
XM_005271326.4:c.1425+29_1425+35del	XP_005271383.1:n.1425+29_1425+35del
XM_005271327.4:c.1242+29_1242+35del	XP_005271384.1:n.1242+29_1242+35del
NM_001172309.2:c.1467+29_1467+35del	NP_001165780.1:n.1467+29_1467+35del
NM_144573.4:c.1659+29_1659+35del MANE Select	NP_653174.3:n.1659+29_1659+35del