Canonical Allele Identifier: CA919034

Gene: NEXN

Linked Data

• dbSNP Id: rs755826752
• ExAC: 1:78408538 ATTAAT / A
• gnomAD v4: 1-77942853-ATTAAT-A
• MyVariant Identifiers: chr1:g.78408539_78408543del (hg19) ; chr1:g.77942854_77942858del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942856_77942860del , CM000663.2:g.77942856_77942860del	GRCh38
NC_000001.10:g.78408541_78408545del , CM000663.1:g.78408541_78408545del	GRCh37
NC_000001.9:g.78181129_78181133del	NCBI36
NG_016625.1:g.59342_59346del , LRG_442:g.59342_59346del
NG_033243.2:g.41236_41240del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.*27_*31del MANE Select	ENSP00000333938.7:n.*27_*31del
ENST00000330010.12:c.*27_*31del	ENSP00000327363.8:n.*27_*31del
ENST00000334785.11:c.*27_*31del	ENSP00000333938.7:n.*27_*31del
ENST00000342754.5:c.1716+38_1717-40del
ENST00000480732.2:n.1629_1633del
NM_001172309.1:c.*27_*31del	NP_001165780.1:n.*27_*31del
NM_144573.3:c.*27_*31del , LRG_442t1:c.*27_*31del	NP_653174.3:n.*27_*31del
XM_005271322.2:c.2017+38_2018-40del	XP_005271379.1:n.2017+38_2018-40del
XM_005271323.2:c.1975+38_1976-40del	XP_005271380.1:n.1975+38_1976-40del
XM_005271324.3:c.1825+38_1826-40del	XP_005271381.1:n.1825+38_1826-40del
XM_005271325.2:c.1795+38_1796-40del	XP_005271382.1:n.1795+38_1796-40del
XM_005271326.2:c.1783+38_1784-40del	XP_005271383.1:n.1783+38_1784-40del
XM_005271327.2:c.1600+38_1601-40del	XP_005271384.1:n.1600+38_1601-40del
XM_005271322.4:c.2017+38_2018-40del	XP_005271379.1:n.2017+38_2018-40del
XM_005271323.4:c.1975+38_1976-40del	XP_005271380.1:n.1975+38_1976-40del
XM_005271324.5:c.1825+38_1826-40del	XP_005271381.1:n.1825+38_1826-40del
XM_005271325.4:c.1795+38_1796-40del	XP_005271382.1:n.1795+38_1796-40del
XM_005271326.4:c.1783+38_1784-40del	XP_005271383.1:n.1783+38_1784-40del
XM_005271327.4:c.1600+38_1601-40del	XP_005271384.1:n.1600+38_1601-40del
NM_001172309.2:c.*27_*31del	NP_001165780.1:n.*27_*31del
NM_144573.4:c.*27_*31del MANE Select	NP_653174.3:n.*27_*31del