Canonical Allele Identifier: CA1177628321

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77935970_77935973delinsATAG , CM000663.2:g.77935970_77935973delinsATAG	GRCh38
NC_000001.10:g.78401655_78401658delinsATAG , CM000663.1:g.78401655_78401658delinsATAG	GRCh37
NC_000001.9:g.78174243_78174246delinsATAG	NCBI36
NG_016625.1:g.52456_52459delinsATAG , LRG_442:g.52456_52459delinsATAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1399_1402delinsATAG MANE Select	ENSP00000333938.7:p.Ile467=
ENST00000330010.12:c.1207_1210delinsATAG	ENSP00000327363.8:p.Ile403=
ENST00000334785.11:c.1399_1402delinsATAG	ENSP00000333938.7:p.Ile467=
ENST00000342754.5:c.1098_1101delinsATAG
ENST00000480732.2:n.973_976delinsATAG
NM_001172309.1:c.1207_1210delinsATAG	NP_001165780.1:p.Ile403=
NM_144573.3:c.1399_1402delinsATAG , LRG_442t1:c.1399_1402delinsATAG	NP_653174.3:p.Ile467=
XM_005271322.2:c.1399_1402delinsATAG	XP_005271379.1:p.Ile467=
XM_005271323.2:c.1357_1360delinsATAG	XP_005271380.1:p.Ile453=
XM_005271324.3:c.1207_1210delinsATAG	XP_005271381.1:p.Ile403=
XM_005271325.2:c.1251+2491_1251+2494delinsATAG	XP_005271382.1:n.1251+2491_1251+2494delinsATAG
XM_005271326.2:c.1165_1168delinsATAG	XP_005271383.1:p.Ile389=
XM_005271327.2:c.982_985delinsATAG	XP_005271384.1:p.Ile328=
XM_005271322.4:c.1399_1402delinsATAG	XP_005271379.1:p.Ile467=
XM_005271323.4:c.1357_1360delinsATAG	XP_005271380.1:p.Ile453=
XM_005271324.5:c.1207_1210delinsATAG	XP_005271381.1:p.Ile403=
XM_005271325.4:c.1251+2491_1251+2494delinsATAG	XP_005271382.1:n.1251+2491_1251+2494delinsATAG
XM_005271326.4:c.1165_1168delinsATAG	XP_005271383.1:p.Ile389=
XM_005271327.4:c.982_985delinsATAG	XP_005271384.1:p.Ile328=
NM_001172309.2:c.1207_1210delinsATAG	NP_001165780.1:p.Ile403=
NM_144573.4:c.1399_1402delinsATAG MANE Select	NP_653174.3:p.Ile467=