Canonical Allele Identifier: CA1177628372

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77936083_77936086delinsAATG , CM000663.2:g.77936083_77936086delinsAATG	GRCh38
NC_000001.10:g.78401768_78401771delinsAATG , CM000663.1:g.78401768_78401771delinsAATG	GRCh37
NC_000001.9:g.78174356_78174359delinsAATG	NCBI36
NG_016625.1:g.52569_52572delinsAATG , LRG_442:g.52569_52572delinsAATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1473+39_1473+42delinsAATG MANE Select	ENSP00000333938.7:n.1473+39_1473+42delinsAATG
ENST00000330010.12:c.1281+39_1281+42delinsAATG	ENSP00000327363.8:n.1281+39_1281+42delinsAATG
ENST00000334785.11:c.1473+39_1473+42delinsAATG	ENSP00000333938.7:n.1473+39_1473+42delinsAATG
ENST00000342754.5:c.1172+39_1172+42delinsAATG
ENST00000480732.2:n.1047+39_1047+42delinsAATG
NM_001172309.1:c.1281+39_1281+42delinsAATG	NP_001165780.1:n.1281+39_1281+42delinsAATG
NM_144573.3:c.1473+39_1473+42delinsAATG , LRG_442t1:c.1473+39_1473+42delinsAATG	NP_653174.3:n.1473+39_1473+42delinsAATG
XM_005271322.2:c.1473+39_1473+42delinsAATG	XP_005271379.1:n.1473+39_1473+42delinsAATG
XM_005271323.2:c.1431+39_1431+42delinsAATG	XP_005271380.1:n.1431+39_1431+42delinsAATG
XM_005271324.3:c.1281+39_1281+42delinsAATG	XP_005271381.1:n.1281+39_1281+42delinsAATG
XM_005271325.2:c.1251+2604_1251+2607delinsAATG	XP_005271382.1:n.1251+2604_1251+2607delinsAATG
XM_005271326.2:c.1239+39_1239+42delinsAATG	XP_005271383.1:n.1239+39_1239+42delinsAATG
XM_005271327.2:c.1056+39_1056+42delinsAATG	XP_005271384.1:n.1056+39_1056+42delinsAATG
XM_005271322.4:c.1473+39_1473+42delinsAATG	XP_005271379.1:n.1473+39_1473+42delinsAATG
XM_005271323.4:c.1431+39_1431+42delinsAATG	XP_005271380.1:n.1431+39_1431+42delinsAATG
XM_005271324.5:c.1281+39_1281+42delinsAATG	XP_005271381.1:n.1281+39_1281+42delinsAATG
XM_005271325.4:c.1251+2604_1251+2607delinsAATG	XP_005271382.1:n.1251+2604_1251+2607delinsAATG
XM_005271326.4:c.1239+39_1239+42delinsAATG	XP_005271383.1:n.1239+39_1239+42delinsAATG
XM_005271327.4:c.1056+39_1056+42delinsAATG	XP_005271384.1:n.1056+39_1056+42delinsAATG
NM_001172309.2:c.1281+39_1281+42delinsAATG	NP_001165780.1:n.1281+39_1281+42delinsAATG
NM_144573.4:c.1473+39_1473+42delinsAATG MANE Select	NP_653174.3:n.1473+39_1473+42delinsAATG