Canonical Allele Identifier: CA918949

Gene: NEXN

Linked Data

• dbSNP Id: rs746537260
• ExAC: 1:78407922 CA / C
• gnomAD v2: 1-78407922-CA-C
• gnomAD v4: 1-77942237-CA-C
• MyVariant Identifiers: chr1:g.78407923del (hg19) ; chr1:g.77942238del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942240del , CM000663.2:g.77942240del	GRCh38
NC_000001.10:g.78407925del , CM000663.1:g.78407925del	GRCh37
NC_000001.9:g.78180513del	NCBI36
NG_016625.1:g.58726del , LRG_442:g.58726del
NG_033243.2:g.41856del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1659+32del MANE Select	ENSP00000333938.7:n.1659+32del
ENST00000330010.12:c.1467+32del	ENSP00000327363.8:n.1467+32del
ENST00000334785.11:c.1659+32del	ENSP00000333938.7:n.1659+32del
ENST00000342754.5:c.1358+32del
ENST00000470735.1:n.498+32del
ENST00000480732.2:n.1233+32del
NM_001172309.1:c.1467+32del	NP_001165780.1:n.1467+32del
NM_144573.3:c.1659+32del , LRG_442t1:c.1659+32del	NP_653174.3:n.1659+32del
XM_005271322.2:c.1659+32del	XP_005271379.1:n.1659+32del
XM_005271323.2:c.1617+32del	XP_005271380.1:n.1617+32del
XM_005271324.3:c.1467+32del	XP_005271381.1:n.1467+32del
XM_005271325.2:c.1437+32del	XP_005271382.1:n.1437+32del
XM_005271326.2:c.1425+32del	XP_005271383.1:n.1425+32del
XM_005271327.2:c.1242+32del	XP_005271384.1:n.1242+32del
XM_005271322.4:c.1659+32del	XP_005271379.1:n.1659+32del
XM_005271323.4:c.1617+32del	XP_005271380.1:n.1617+32del
XM_005271324.5:c.1467+32del	XP_005271381.1:n.1467+32del
XM_005271325.4:c.1437+32del	XP_005271382.1:n.1437+32del
XM_005271326.4:c.1425+32del	XP_005271383.1:n.1425+32del
XM_005271327.4:c.1242+32del	XP_005271384.1:n.1242+32del
NM_001172309.2:c.1467+32del	NP_001165780.1:n.1467+32del
NM_144573.4:c.1659+32del MANE Select	NP_653174.3:n.1659+32del