Canonical Allele Identifier: CA24686283

Gene: NEXN

Linked Data

• ClinVar Variation Id: 1584554
• ClinVar RCV Id: RCV002102678
• dbSNP Id: rs935328552
• gnomAD v2: 1-78401490-TATTA-T
• gnomAD v4: 1-77935805-TATTA-T
• MyVariant Identifiers: chr1:g.78401491_78401494del (hg19) ; chr1:g.77935806_77935809del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77935809_77935812del , CM000663.2:g.77935809_77935812del	GRCh38
NC_000001.10:g.78401494_78401497del , CM000663.1:g.78401494_78401497del	GRCh37
NC_000001.9:g.78174082_78174085del	NCBI36
NG_016625.1:g.52295_52298del , LRG_442:g.52295_52298del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1252-14_1252-11del MANE Select	ENSP00000333938.7:n.1252-14_1252-11del
ENST00000330010.12:c.1060-14_1060-11del	ENSP00000327363.8:n.1060-14_1060-11del
ENST00000334785.11:c.1252-14_1252-11del	ENSP00000333938.7:n.1252-14_1252-11del
ENST00000342754.5:c.951-14_951-11del
ENST00000440324.5:c.1210-14_1210-11del	ENSP00000411902.1:n.1210-14_1210-11del
ENST00000464998.1:n.712-14_712-11del
ENST00000480732.2:n.826-14_826-11del
NM_001172309.1:c.1060-14_1060-11del	NP_001165780.1:n.1060-14_1060-11del
NM_144573.3:c.1252-14_1252-11del , LRG_442t1:c.1252-14_1252-11del	NP_653174.3:n.1252-14_1252-11del
XM_005271322.2:c.1252-14_1252-11del	XP_005271379.1:n.1252-14_1252-11del
XM_005271323.2:c.1210-14_1210-11del	XP_005271380.1:n.1210-14_1210-11del
XM_005271324.3:c.1060-14_1060-11del	XP_005271381.1:n.1060-14_1060-11del
XM_005271325.2:c.1251+2330_1251+2333del	XP_005271382.1:n.1251+2330_1251+2333del
XM_005271326.2:c.1018-14_1018-11del	XP_005271383.1:n.1018-14_1018-11del
XM_005271327.2:c.835-14_835-11del	XP_005271384.1:n.835-14_835-11del
XM_005271322.4:c.1252-14_1252-11del	XP_005271379.1:n.1252-14_1252-11del
XM_005271323.4:c.1210-14_1210-11del	XP_005271380.1:n.1210-14_1210-11del
XM_005271324.5:c.1060-14_1060-11del	XP_005271381.1:n.1060-14_1060-11del
XM_005271325.4:c.1251+2330_1251+2333del	XP_005271382.1:n.1251+2330_1251+2333del
XM_005271326.4:c.1018-14_1018-11del	XP_005271383.1:n.1018-14_1018-11del
XM_005271327.4:c.835-14_835-11del	XP_005271384.1:n.835-14_835-11del
NM_001172309.2:c.1060-14_1060-11del	NP_001165780.1:n.1060-14_1060-11del
NM_144573.4:c.1252-14_1252-11del MANE Select	NP_653174.3:n.1252-14_1252-11del