Canonical Allele Identifier: CA1177628098

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77935464_77935485delinsCCATATTTCCTAATGAGAATAG , CM000663.2:g.77935464_77935485delinsCCATATTTCCTAATGAGAATAG	GRCh38
NC_000001.10:g.78401149_78401170delinsCCATATTTCCTAATGAGAATAG , CM000663.1:g.78401149_78401170delinsCCATATTTCCTAATGAGAATAG	GRCh37
NC_000001.9:g.78173737_78173758delinsCCATATTTCCTAATGAGAATAG	NCBI36
NG_016625.1:g.51950_51971delinsCCATATTTCCTAATGAGAATAG , LRG_442:g.51950_51971delinsCCATATTTCCTAATGAGAATAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1252-359_1252-338delinsCCATATTTCCTAATGAGAATAG MANE Select	ENSP00000333938.7:n.1252-359_1252-338delinsCCATATTTCCTAATGAGA...
ENST00000330010.12:c.1060-359_1060-338delinsCCATATTTCCTAATGAGAATAG	ENSP00000327363.8:n.1060-359_1060-338delinsCCATATTTCCTAATGAGA...
ENST00000334785.11:c.1252-359_1252-338delinsCCATATTTCCTAATGAGAATAG	ENSP00000333938.7:n.1252-359_1252-338delinsCCATATTTCCTAATGAGA...
ENST00000342754.5:c.951-359_951-338delinsCCATATTTCCTAATGAGAATAG
ENST00000440324.5:c.1210-359_1210-338delinsCCATATTTCCTAATGAGAATAG	ENSP00000411902.1:n.1210-359_1210-338delinsCCATATTTCCTAATGAGA...
ENST00000464998.1:n.712-359_712-338delinsCCATATTTCCTAATGAGAATAG
ENST00000480732.2:n.826-359_826-338delinsCCATATTTCCTAATGAGAATAG
NM_001172309.1:c.1060-359_1060-338delinsCCATATTTCCTAATGAGAATAG	NP_001165780.1:n.1060-359_1060-338delinsCCATATTTCCTAATGAGAATA...
NM_144573.3:c.1252-359_1252-338delinsCCATATTTCCTAATGAGAATAG , LRG_442t1:c.1252-359_1252-338delinsCCATATTTCCTAATGAGAATAG	NP_653174.3:n.1252-359_1252-338delinsCCATATTTCCTAATGAGAATAG
XM_005271322.2:c.1252-359_1252-338delinsCCATATTTCCTAATGAGAATAG	XP_005271379.1:n.1252-359_1252-338delinsCCATATTTCCTAATGAGAATA...
XM_005271323.2:c.1210-359_1210-338delinsCCATATTTCCTAATGAGAATAG	XP_005271380.1:n.1210-359_1210-338delinsCCATATTTCCTAATGAGAATA...
XM_005271324.3:c.1060-359_1060-338delinsCCATATTTCCTAATGAGAATAG	XP_005271381.1:n.1060-359_1060-338delinsCCATATTTCCTAATGAGAATA...
XM_005271325.2:c.1251+1985_1251+2006delinsCCATATTTCCTAATGAGAATAG	XP_005271382.1:n.1251+1985_1251+2006delinsCCATATTTCCTAATGAGAA...
XM_005271326.2:c.1018-359_1018-338delinsCCATATTTCCTAATGAGAATAG	XP_005271383.1:n.1018-359_1018-338delinsCCATATTTCCTAATGAGAATA...
XM_005271327.2:c.835-359_835-338delinsCCATATTTCCTAATGAGAATAG	XP_005271384.1:n.835-359_835-338delinsCCATATTTCCTAATGAGAATAG
XM_005271322.4:c.1252-359_1252-338delinsCCATATTTCCTAATGAGAATAG	XP_005271379.1:n.1252-359_1252-338delinsCCATATTTCCTAATGAGAATA...
XM_005271323.4:c.1210-359_1210-338delinsCCATATTTCCTAATGAGAATAG	XP_005271380.1:n.1210-359_1210-338delinsCCATATTTCCTAATGAGAATA...
XM_005271324.5:c.1060-359_1060-338delinsCCATATTTCCTAATGAGAATAG	XP_005271381.1:n.1060-359_1060-338delinsCCATATTTCCTAATGAGAATA...
XM_005271325.4:c.1251+1985_1251+2006delinsCCATATTTCCTAATGAGAATAG	XP_005271382.1:n.1251+1985_1251+2006delinsCCATATTTCCTAATGAGAA...
XM_005271326.4:c.1018-359_1018-338delinsCCATATTTCCTAATGAGAATAG	XP_005271383.1:n.1018-359_1018-338delinsCCATATTTCCTAATGAGAATA...
XM_005271327.4:c.835-359_835-338delinsCCATATTTCCTAATGAGAATAG	XP_005271384.1:n.835-359_835-338delinsCCATATTTCCTAATGAGAATAG
NM_001172309.2:c.1060-359_1060-338delinsCCATATTTCCTAATGAGAATAG	NP_001165780.1:n.1060-359_1060-338delinsCCATATTTCCTAATGAGAATA...
NM_144573.4:c.1252-359_1252-338delinsCCATATTTCCTAATGAGAATAG MANE Select	NP_653174.3:n.1252-359_1252-338delinsCCATATTTCCTAATGAGAATAG