Canonical Allele Identifier: CA2646275743

Gene: NEXN

Linked Data

• gnomAD v4: 1-77942857-ATTTTT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942862_77942866del , CM000663.2:g.77942862_77942866del	GRCh38
NC_000001.10:g.78408547_78408551del , CM000663.1:g.78408547_78408551del	GRCh37
NC_000001.9:g.78181135_78181139del	NCBI36
NG_016625.1:g.59348_59352del , LRG_442:g.59348_59352del
NG_033243.2:g.41232_41236del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.*33_*37del MANE Select	ENSP00000333938.7:n.*33_*37del
ENST00000330010.12:c.*33_*37del	ENSP00000327363.8:n.*33_*37del
ENST00000334785.11:c.*33_*37del	ENSP00000333938.7:n.*33_*37del
ENST00000342754.5:c.1717-38_1717-34del
ENST00000480732.2:n.1635_1639del
NM_001172309.1:c.*33_*37del	NP_001165780.1:n.*33_*37del
NM_144573.3:c.*33_*37del , LRG_442t1:c.*33_*37del	NP_653174.3:n.*33_*37del
XM_005271322.2:c.2018-38_2018-34del	XP_005271379.1:n.2018-38_2018-34del
XM_005271323.2:c.1976-38_1976-34del	XP_005271380.1:n.1976-38_1976-34del
XM_005271324.3:c.1826-38_1826-34del	XP_005271381.1:n.1826-38_1826-34del
XM_005271325.2:c.1796-38_1796-34del	XP_005271382.1:n.1796-38_1796-34del
XM_005271326.2:c.1784-38_1784-34del	XP_005271383.1:n.1784-38_1784-34del
XM_005271327.2:c.1601-38_1601-34del	XP_005271384.1:n.1601-38_1601-34del
XM_005271322.4:c.2018-38_2018-34del	XP_005271379.1:n.2018-38_2018-34del
XM_005271323.4:c.1976-38_1976-34del	XP_005271380.1:n.1976-38_1976-34del
XM_005271324.5:c.1826-38_1826-34del	XP_005271381.1:n.1826-38_1826-34del
XM_005271325.4:c.1796-38_1796-34del	XP_005271382.1:n.1796-38_1796-34del
XM_005271326.4:c.1784-38_1784-34del	XP_005271383.1:n.1784-38_1784-34del
XM_005271327.4:c.1601-38_1601-34del	XP_005271384.1:n.1601-38_1601-34del
NM_001172309.2:c.*33_*37del	NP_001165780.1:n.*33_*37del
NM_144573.4:c.*33_*37del MANE Select	NP_653174.3:n.*33_*37del