Canonical Allele Identifier: CA1177628301

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77935917_77935921delinsAAAGC , CM000663.2:g.77935917_77935921delinsAAAGC	GRCh38
NC_000001.10:g.78401602_78401606delinsAAAGC , CM000663.1:g.78401602_78401606delinsAAAGC	GRCh37
NC_000001.9:g.78174190_78174194delinsAAAGC	NCBI36
NG_016625.1:g.52403_52407delinsAAAGC , LRG_442:g.52403_52407delinsAAAGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1346_1350delinsAAAGC MANE Select	ENSP00000333938.7:p.Lys449=
ENST00000330010.12:c.1154_1158delinsAAAGC	ENSP00000327363.8:p.Lys385=
ENST00000334785.11:c.1346_1350delinsAAAGC	ENSP00000333938.7:p.Lys449=
ENST00000342754.5:c.1045_1049delinsAAAGC
ENST00000464998.1:n.806_810delinsAAAGC
ENST00000480732.2:n.920_924delinsAAAGC
NM_001172309.1:c.1154_1158delinsAAAGC	NP_001165780.1:p.Lys385=
NM_144573.3:c.1346_1350delinsAAAGC , LRG_442t1:c.1346_1350delinsAAAGC	NP_653174.3:p.Lys449=
XM_005271322.2:c.1346_1350delinsAAAGC	XP_005271379.1:p.Lys449=
XM_005271323.2:c.1304_1308delinsAAAGC	XP_005271380.1:p.Lys435=
XM_005271324.3:c.1154_1158delinsAAAGC	XP_005271381.1:p.Lys385=
XM_005271325.2:c.1251+2438_1251+2442delinsAAAGC	XP_005271382.1:n.1251+2438_1251+2442delinsAAAGC
XM_005271326.2:c.1112_1116delinsAAAGC	XP_005271383.1:p.Lys371=
XM_005271327.2:c.929_933delinsAAAGC	XP_005271384.1:p.Lys310=
XM_005271322.4:c.1346_1350delinsAAAGC	XP_005271379.1:p.Lys449=
XM_005271323.4:c.1304_1308delinsAAAGC	XP_005271380.1:p.Lys435=
XM_005271324.5:c.1154_1158delinsAAAGC	XP_005271381.1:p.Lys385=
XM_005271325.4:c.1251+2438_1251+2442delinsAAAGC	XP_005271382.1:n.1251+2438_1251+2442delinsAAAGC
XM_005271326.4:c.1112_1116delinsAAAGC	XP_005271383.1:p.Lys371=
XM_005271327.4:c.929_933delinsAAAGC	XP_005271384.1:p.Lys310=
NM_001172309.2:c.1154_1158delinsAAAGC	NP_001165780.1:p.Lys385=
NM_144573.4:c.1346_1350delinsAAAGC MANE Select	NP_653174.3:p.Lys449=