Canonical Allele Identifier: CA524231118

Gene: NEXN

Linked Data

• dbSNP Id: rs756441030
• gnomAD v2: 1-78399172-T-TC
• MyVariant Identifiers: chr1:g.78399172_78399173insC (hg19) ; chr1:g.77933487_77933488insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77933487_77933488insC , CM000663.2:g.77933487_77933488insC	GRCh38
NC_000001.10:g.78399172_78399173insC , CM000663.1:g.78399172_78399173insC	GRCh37
NC_000001.9:g.78171760_78171761insC	NCBI36
NG_016625.1:g.49973_49974insC , LRG_442:g.49973_49974insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1251+8_1251+9insC MANE Select	ENSP00000333938.7:n.1251+8_1251+9insC
ENST00000330010.12:c.1059+8_1059+9insC	ENSP00000327363.8:n.1059+8_1059+9insC
ENST00000334785.11:c.1251+8_1251+9insC	ENSP00000333938.7:n.1251+8_1251+9insC
ENST00000342754.5:c.950+8_950+9insC
ENST00000440324.5:c.1209+8_1209+9insC	ENSP00000411902.1:n.1209+8_1209+9insC
ENST00000464998.1:n.711+8_711+9insC
ENST00000480732.2:n.825+8_825+9insC
NM_001172309.1:c.1059+8_1059+9insC	NP_001165780.1:n.1059+8_1059+9insC
NM_144573.3:c.1251+8_1251+9insC , LRG_442t1:c.1251+8_1251+9insC	NP_653174.3:n.1251+8_1251+9insC
XM_005271322.2:c.1251+8_1251+9insC	XP_005271379.1:n.1251+8_1251+9insC
XM_005271323.2:c.1209+8_1209+9insC	XP_005271380.1:n.1209+8_1209+9insC
XM_005271324.3:c.1059+8_1059+9insC	XP_005271381.1:n.1059+8_1059+9insC
XM_005271325.2:c.1251+8_1251+9insC	XP_005271382.1:n.1251+8_1251+9insC
XM_005271326.2:c.1017+8_1017+9insC	XP_005271383.1:n.1017+8_1017+9insC
XM_005271327.2:c.834+8_834+9insC	XP_005271384.1:n.834+8_834+9insC
XM_005271322.4:c.1251+8_1251+9insC	XP_005271379.1:n.1251+8_1251+9insC
XM_005271323.4:c.1209+8_1209+9insC	XP_005271380.1:n.1209+8_1209+9insC
XM_005271324.5:c.1059+8_1059+9insC	XP_005271381.1:n.1059+8_1059+9insC
XM_005271325.4:c.1251+8_1251+9insC	XP_005271382.1:n.1251+8_1251+9insC
XM_005271326.4:c.1017+8_1017+9insC	XP_005271383.1:n.1017+8_1017+9insC
XM_005271327.4:c.834+8_834+9insC	XP_005271384.1:n.834+8_834+9insC
NM_001172309.2:c.1059+8_1059+9insC	NP_001165780.1:n.1059+8_1059+9insC
NM_144573.4:c.1251+8_1251+9insC MANE Select	NP_653174.3:n.1251+8_1251+9insC