Canonical Allele Identifier: CA1177620184

Gene: NEXN

Linked Data

• dbSNP Id: rs1430077296
• gnomAD v4: 1-77917800-AT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77917806del , CM000663.2:g.77917806del	GRCh38
NC_000001.10:g.78383491del , CM000663.1:g.78383491del	GRCh37
NC_000001.9:g.78156079del	NCBI36
NG_016625.1:g.34292del , LRG_442:g.34292del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.219+49del MANE Select	ENSP00000333938.7:n.219+49del
ENST00000330010.12:c.28-154del	ENSP00000327363.8:n.28-154del
ENST00000334785.11:c.219+49del	ENSP00000333938.7:n.219+49del
ENST00000401035.7:c.28-154del	ENSP00000383814.3:n.28-154del
ENST00000440324.5:c.219+49del	ENSP00000411902.1:n.219+49del
NM_001172309.1:c.28-154del	NP_001165780.1:n.28-154del
NM_144573.3:c.219+49del , LRG_442t1:c.219+49del	NP_653174.3:n.219+49del
XM_005271322.2:c.219+49del	XP_005271379.1:n.219+49del
XM_005271323.2:c.219+49del	XP_005271380.1:n.219+49del
XM_005271324.3:c.28-154del	XP_005271381.1:n.28-154del
XM_005271325.2:c.219+49del	XP_005271382.1:n.219+49del
XM_005271326.2:c.28-154del	XP_005271383.1:n.28-154del
XM_005271327.2:c.219+49del	XP_005271384.1:n.219+49del
XM_005271322.4:c.219+49del	XP_005271379.1:n.219+49del
XM_005271323.4:c.219+49del	XP_005271380.1:n.219+49del
XM_005271324.5:c.28-154del	XP_005271381.1:n.28-154del
XM_005271325.4:c.219+49del	XP_005271382.1:n.219+49del
XM_005271326.4:c.28-154del	XP_005271383.1:n.28-154del
XM_005271327.4:c.219+49del	XP_005271384.1:n.219+49del
NM_001172309.2:c.28-154del	NP_001165780.1:n.28-154del
NM_144573.4:c.219+49del MANE Select	NP_653174.3:n.219+49del