Canonical Allele Identifier: CA524230988

Gene: NEXN

Linked Data

• dbSNP Id: rs1322783551
• gnomAD v2: 1-78401487-ACT-A
• gnomAD v4: 1-77935802-ACT-A
• MyVariant Identifiers: chr1:g.78401488_78401489del (hg19) ; chr1:g.77935803_77935804del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77935803_77935804del , CM000663.2:g.77935803_77935804del	GRCh38
NC_000001.10:g.78401488_78401489del , CM000663.1:g.78401488_78401489del	GRCh37
NC_000001.9:g.78174076_78174077del	NCBI36
NG_016625.1:g.52289_52290del , LRG_442:g.52289_52290del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1252-20_1252-19del MANE Select	ENSP00000333938.7:n.1252-20_1252-19del
ENST00000330010.12:c.1060-20_1060-19del	ENSP00000327363.8:n.1060-20_1060-19del
ENST00000334785.11:c.1252-20_1252-19del	ENSP00000333938.7:n.1252-20_1252-19del
ENST00000342754.5:c.951-20_951-19del
ENST00000440324.5:c.1210-20_1210-19del	ENSP00000411902.1:n.1210-20_1210-19del
ENST00000464998.1:n.712-20_712-19del
ENST00000480732.2:n.826-20_826-19del
NM_001172309.1:c.1060-20_1060-19del	NP_001165780.1:n.1060-20_1060-19del
NM_144573.3:c.1252-20_1252-19del , LRG_442t1:c.1252-20_1252-19del	NP_653174.3:n.1252-20_1252-19del
XM_005271322.2:c.1252-20_1252-19del	XP_005271379.1:n.1252-20_1252-19del
XM_005271323.2:c.1210-20_1210-19del	XP_005271380.1:n.1210-20_1210-19del
XM_005271324.3:c.1060-20_1060-19del	XP_005271381.1:n.1060-20_1060-19del
XM_005271325.2:c.1251+2324_1251+2325del	XP_005271382.1:n.1251+2324_1251+2325del
XM_005271326.2:c.1018-20_1018-19del	XP_005271383.1:n.1018-20_1018-19del
XM_005271327.2:c.835-20_835-19del	XP_005271384.1:n.835-20_835-19del
XM_005271322.4:c.1252-20_1252-19del	XP_005271379.1:n.1252-20_1252-19del
XM_005271323.4:c.1210-20_1210-19del	XP_005271380.1:n.1210-20_1210-19del
XM_005271324.5:c.1060-20_1060-19del	XP_005271381.1:n.1060-20_1060-19del
XM_005271325.4:c.1251+2324_1251+2325del	XP_005271382.1:n.1251+2324_1251+2325del
XM_005271326.4:c.1018-20_1018-19del	XP_005271383.1:n.1018-20_1018-19del
XM_005271327.4:c.835-20_835-19del	XP_005271384.1:n.835-20_835-19del
NM_001172309.2:c.1060-20_1060-19del	NP_001165780.1:n.1060-20_1060-19del
NM_144573.4:c.1252-20_1252-19del MANE Select	NP_653174.3:n.1252-20_1252-19del