Canonical Allele Identifier: CA24705092

Gene: NEXN

Linked Data

• dbSNP Id: rs1010735153
• gnomAD v4: 1-77917495-TTATC-T
• MyVariant Identifiers: chr1:g.78383181_78383184del (hg19) ; chr1:g.77917496_77917499del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77917501_77917504del , CM000663.2:g.77917501_77917504del	GRCh38
NC_000001.10:g.78383186_78383189del , CM000663.1:g.78383186_78383189del	GRCh37
NC_000001.9:g.78155774_78155777del	NCBI36
NG_016625.1:g.33987_33990del , LRG_442:g.33987_33990del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.28-65_28-62del MANE Select	ENSP00000333938.7:n.28-65_28-62del
ENST00000330010.12:c.28-459_28-456del	ENSP00000327363.8:n.28-459_28-456del
ENST00000334785.11:c.28-65_28-62del	ENSP00000333938.7:n.28-65_28-62del
ENST00000401035.7:c.28-459_28-456del	ENSP00000383814.3:n.28-459_28-456del
ENST00000440324.5:c.28-65_28-62del	ENSP00000411902.1:n.28-65_28-62del
NM_001172309.1:c.28-459_28-456del	NP_001165780.1:n.28-459_28-456del
NM_144573.3:c.28-65_28-62del , LRG_442t1:c.28-65_28-62del	NP_653174.3:n.28-65_28-62del
XM_005271322.2:c.28-65_28-62del	XP_005271379.1:n.28-65_28-62del
XM_005271323.2:c.28-65_28-62del	XP_005271380.1:n.28-65_28-62del
XM_005271324.3:c.28-459_28-456del	XP_005271381.1:n.28-459_28-456del
XM_005271325.2:c.28-65_28-62del	XP_005271382.1:n.28-65_28-62del
XM_005271326.2:c.28-459_28-456del	XP_005271383.1:n.28-459_28-456del
XM_005271327.2:c.28-65_28-62del	XP_005271384.1:n.28-65_28-62del
XM_005271322.4:c.28-65_28-62del	XP_005271379.1:n.28-65_28-62del
XM_005271323.4:c.28-65_28-62del	XP_005271380.1:n.28-65_28-62del
XM_005271324.5:c.28-459_28-456del	XP_005271381.1:n.28-459_28-456del
XM_005271325.4:c.28-65_28-62del	XP_005271382.1:n.28-65_28-62del
XM_005271326.4:c.28-459_28-456del	XP_005271383.1:n.28-459_28-456del
XM_005271327.4:c.28-65_28-62del	XP_005271384.1:n.28-65_28-62del
NM_001172309.2:c.28-459_28-456del	NP_001165780.1:n.28-459_28-456del
NM_144573.4:c.28-65_28-62del MANE Select	NP_653174.3:n.28-65_28-62del