Canonical Allele Identifier: CA2544569309

Gene: NEXN

Linked Data

• gnomAD v4: 1-77933207-CAGTTTCTTCAAGAAATAGTCCCTTTTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77933211_77933237del , CM000663.2:g.77933211_77933237del	GRCh38
NC_000001.10:g.78398896_78398922del , CM000663.1:g.78398896_78398922del	GRCh37
NC_000001.9:g.78171484_78171510del	NCBI36
NG_016625.1:g.49697_49723del , LRG_442:g.49697_49723del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1054-71_1054-45del MANE Select	ENSP00000333938.7:n.1054-71_1054-45del
ENST00000330010.12:c.862-71_862-45del	ENSP00000327363.8:n.862-71_862-45del
ENST00000334785.11:c.1054-71_1054-45del	ENSP00000333938.7:n.1054-71_1054-45del
ENST00000342754.5:c.753-71_753-45del
ENST00000401035.7:c.862-71_862-45del	ENSP00000383814.3:n.862-71_862-45del
ENST00000440324.5:c.1012-71_1012-45del	ENSP00000411902.1:n.1012-71_1012-45del
ENST00000464998.1:n.514-71_514-45del
ENST00000480732.2:n.557_583del
NM_001172309.1:c.862-71_862-45del	NP_001165780.1:n.862-71_862-45del
NM_144573.3:c.1054-71_1054-45del , LRG_442t1:c.1054-71_1054-45del	NP_653174.3:n.1054-71_1054-45del
XM_005271322.2:c.1054-71_1054-45del	XP_005271379.1:n.1054-71_1054-45del
XM_005271323.2:c.1012-71_1012-45del	XP_005271380.1:n.1012-71_1012-45del
XM_005271324.3:c.862-71_862-45del	XP_005271381.1:n.862-71_862-45del
XM_005271325.2:c.1054-71_1054-45del	XP_005271382.1:n.1054-71_1054-45del
XM_005271326.2:c.820-71_820-45del	XP_005271383.1:n.820-71_820-45del
XM_005271327.2:c.637-71_637-45del	XP_005271384.1:n.637-71_637-45del
XM_005271322.4:c.1054-71_1054-45del	XP_005271379.1:n.1054-71_1054-45del
XM_005271323.4:c.1012-71_1012-45del	XP_005271380.1:n.1012-71_1012-45del
XM_005271324.5:c.862-71_862-45del	XP_005271381.1:n.862-71_862-45del
XM_005271325.4:c.1054-71_1054-45del	XP_005271382.1:n.1054-71_1054-45del
XM_005271326.4:c.820-71_820-45del	XP_005271383.1:n.820-71_820-45del
XM_005271327.4:c.637-71_637-45del	XP_005271384.1:n.637-71_637-45del
NM_001172309.2:c.862-71_862-45del	NP_001165780.1:n.862-71_862-45del
NM_144573.4:c.1054-71_1054-45del MANE Select	NP_653174.3:n.1054-71_1054-45del