Canonical Allele Identifier: CA1177628450

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77936241_77936243delinsAGT , CM000663.2:g.77936241_77936243delinsAGT	GRCh38
NC_000001.10:g.78401926_78401928delinsAGT , CM000663.1:g.78401926_78401928delinsAGT	GRCh37
NC_000001.9:g.78174514_78174516delinsAGT	NCBI36
NG_016625.1:g.52727_52729delinsAGT , LRG_442:g.52727_52729delinsAGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1473+197_1473+199delinsAGT MANE Select	ENSP00000333938.7:n.1473+197_1473+199delinsAGT
ENST00000330010.12:c.1281+197_1281+199delinsAGT	ENSP00000327363.8:n.1281+197_1281+199delinsAGT
ENST00000334785.11:c.1473+197_1473+199delinsAGT	ENSP00000333938.7:n.1473+197_1473+199delinsAGT
ENST00000342754.5:c.1172+197_1172+199delinsAGT
ENST00000480732.2:n.1047+197_1047+199delinsAGT
NM_001172309.1:c.1281+197_1281+199delinsAGT	NP_001165780.1:n.1281+197_1281+199delinsAGT
NM_144573.3:c.1473+197_1473+199delinsAGT , LRG_442t1:c.1473+197_1473+199delinsAGT	NP_653174.3:n.1473+197_1473+199delinsAGT
XM_005271322.2:c.1473+197_1473+199delinsAGT	XP_005271379.1:n.1473+197_1473+199delinsAGT
XM_005271323.2:c.1431+197_1431+199delinsAGT	XP_005271380.1:n.1431+197_1431+199delinsAGT
XM_005271324.3:c.1281+197_1281+199delinsAGT	XP_005271381.1:n.1281+197_1281+199delinsAGT
XM_005271325.2:c.1251+2762_1251+2764delinsAGT	XP_005271382.1:n.1251+2762_1251+2764delinsAGT
XM_005271326.2:c.1239+197_1239+199delinsAGT	XP_005271383.1:n.1239+197_1239+199delinsAGT
XM_005271327.2:c.1056+197_1056+199delinsAGT	XP_005271384.1:n.1056+197_1056+199delinsAGT
XM_005271322.4:c.1473+197_1473+199delinsAGT	XP_005271379.1:n.1473+197_1473+199delinsAGT
XM_005271323.4:c.1431+197_1431+199delinsAGT	XP_005271380.1:n.1431+197_1431+199delinsAGT
XM_005271324.5:c.1281+197_1281+199delinsAGT	XP_005271381.1:n.1281+197_1281+199delinsAGT
XM_005271325.4:c.1251+2762_1251+2764delinsAGT	XP_005271382.1:n.1251+2762_1251+2764delinsAGT
XM_005271326.4:c.1239+197_1239+199delinsAGT	XP_005271383.1:n.1239+197_1239+199delinsAGT
XM_005271327.4:c.1056+197_1056+199delinsAGT	XP_005271384.1:n.1056+197_1056+199delinsAGT
NM_001172309.2:c.1281+197_1281+199delinsAGT	NP_001165780.1:n.1281+197_1281+199delinsAGT
NM_144573.4:c.1473+197_1473+199delinsAGT MANE Select	NP_653174.3:n.1473+197_1473+199delinsAGT