Canonical Allele Identifier: CA1177628449

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77936240_77936241delinsCA , CM000663.2:g.77936240_77936241delinsCA	GRCh38
NC_000001.10:g.78401925_78401926delinsCA , CM000663.1:g.78401925_78401926delinsCA	GRCh37
NC_000001.9:g.78174513_78174514delinsCA	NCBI36
NG_016625.1:g.52726_52727delinsCA , LRG_442:g.52726_52727delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1473+196_1473+197delinsCA MANE Select	ENSP00000333938.7:n.1473+196_1473+197delinsCA
ENST00000330010.12:c.1281+196_1281+197delinsCA	ENSP00000327363.8:n.1281+196_1281+197delinsCA
ENST00000334785.11:c.1473+196_1473+197delinsCA	ENSP00000333938.7:n.1473+196_1473+197delinsCA
ENST00000342754.5:c.1172+196_1172+197delinsCA
ENST00000480732.2:n.1047+196_1047+197delinsCA
NM_001172309.1:c.1281+196_1281+197delinsCA	NP_001165780.1:n.1281+196_1281+197delinsCA
NM_144573.3:c.1473+196_1473+197delinsCA , LRG_442t1:c.1473+196_1473+197delinsCA	NP_653174.3:n.1473+196_1473+197delinsCA
XM_005271322.2:c.1473+196_1473+197delinsCA	XP_005271379.1:n.1473+196_1473+197delinsCA
XM_005271323.2:c.1431+196_1431+197delinsCA	XP_005271380.1:n.1431+196_1431+197delinsCA
XM_005271324.3:c.1281+196_1281+197delinsCA	XP_005271381.1:n.1281+196_1281+197delinsCA
XM_005271325.2:c.1251+2761_1251+2762delinsCA	XP_005271382.1:n.1251+2761_1251+2762delinsCA
XM_005271326.2:c.1239+196_1239+197delinsCA	XP_005271383.1:n.1239+196_1239+197delinsCA
XM_005271327.2:c.1056+196_1056+197delinsCA	XP_005271384.1:n.1056+196_1056+197delinsCA
XM_005271322.4:c.1473+196_1473+197delinsCA	XP_005271379.1:n.1473+196_1473+197delinsCA
XM_005271323.4:c.1431+196_1431+197delinsCA	XP_005271380.1:n.1431+196_1431+197delinsCA
XM_005271324.5:c.1281+196_1281+197delinsCA	XP_005271381.1:n.1281+196_1281+197delinsCA
XM_005271325.4:c.1251+2761_1251+2762delinsCA	XP_005271382.1:n.1251+2761_1251+2762delinsCA
XM_005271326.4:c.1239+196_1239+197delinsCA	XP_005271383.1:n.1239+196_1239+197delinsCA
XM_005271327.4:c.1056+196_1056+197delinsCA	XP_005271384.1:n.1056+196_1056+197delinsCA
NM_001172309.2:c.1281+196_1281+197delinsCA	NP_001165780.1:n.1281+196_1281+197delinsCA
NM_144573.4:c.1473+196_1473+197delinsCA MANE Select	NP_653174.3:n.1473+196_1473+197delinsCA