Canonical Allele Identifier: CA1177628473

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77936296_77936298delinsAAT , CM000663.2:g.77936296_77936298delinsAAT	GRCh38
NC_000001.10:g.78401981_78401983delinsAAT , CM000663.1:g.78401981_78401983delinsAAT	GRCh37
NC_000001.9:g.78174569_78174571delinsAAT	NCBI36
NG_016625.1:g.52782_52784delinsAAT , LRG_442:g.52782_52784delinsAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1473+252_1473+254delinsAAT MANE Select	ENSP00000333938.7:n.1473+252_1473+254delinsAAT
ENST00000330010.12:c.1281+252_1281+254delinsAAT	ENSP00000327363.8:n.1281+252_1281+254delinsAAT
ENST00000334785.11:c.1473+252_1473+254delinsAAT	ENSP00000333938.7:n.1473+252_1473+254delinsAAT
ENST00000342754.5:c.1172+252_1172+254delinsAAT
ENST00000480732.2:n.1047+252_1047+254delinsAAT
NM_001172309.1:c.1281+252_1281+254delinsAAT	NP_001165780.1:n.1281+252_1281+254delinsAAT
NM_144573.3:c.1473+252_1473+254delinsAAT , LRG_442t1:c.1473+252_1473+254delinsAAT	NP_653174.3:n.1473+252_1473+254delinsAAT
XM_005271322.2:c.1473+252_1473+254delinsAAT	XP_005271379.1:n.1473+252_1473+254delinsAAT
XM_005271323.2:c.1431+252_1431+254delinsAAT	XP_005271380.1:n.1431+252_1431+254delinsAAT
XM_005271324.3:c.1281+252_1281+254delinsAAT	XP_005271381.1:n.1281+252_1281+254delinsAAT
XM_005271325.2:c.1251+2817_1251+2819delinsAAT	XP_005271382.1:n.1251+2817_1251+2819delinsAAT
XM_005271326.2:c.1239+252_1239+254delinsAAT	XP_005271383.1:n.1239+252_1239+254delinsAAT
XM_005271327.2:c.1056+252_1056+254delinsAAT	XP_005271384.1:n.1056+252_1056+254delinsAAT
XM_005271322.4:c.1473+252_1473+254delinsAAT	XP_005271379.1:n.1473+252_1473+254delinsAAT
XM_005271323.4:c.1431+252_1431+254delinsAAT	XP_005271380.1:n.1431+252_1431+254delinsAAT
XM_005271324.5:c.1281+252_1281+254delinsAAT	XP_005271381.1:n.1281+252_1281+254delinsAAT
XM_005271325.4:c.1251+2817_1251+2819delinsAAT	XP_005271382.1:n.1251+2817_1251+2819delinsAAT
XM_005271326.4:c.1239+252_1239+254delinsAAT	XP_005271383.1:n.1239+252_1239+254delinsAAT
XM_005271327.4:c.1056+252_1056+254delinsAAT	XP_005271384.1:n.1056+252_1056+254delinsAAT
NM_001172309.2:c.1281+252_1281+254delinsAAT	NP_001165780.1:n.1281+252_1281+254delinsAAT
NM_144573.4:c.1473+252_1473+254delinsAAT MANE Select	NP_653174.3:n.1473+252_1473+254delinsAAT