Canonical Allele Identifier: CA2580652575

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77935891_77935892del , CM000663.2:g.77935891_77935892del	GRCh38
NC_000001.10:g.78401576_78401577del , CM000663.1:g.78401576_78401577del	GRCh37
NC_000001.9:g.78174164_78174165del	NCBI36
NG_016625.1:g.52377_52378del , LRG_442:g.52377_52378del

Transcript Alleles

HGVS	Amino-acid change
ENST00000334785.12:c.1320_1321del MANE Select	ENSP00000333938.7:p.Ser440ArgfsTer6
ENST00000330010.12:c.1128_1129del	ENSP00000327363.8:p.Ser376ArgfsTer6
ENST00000334785.11:c.1320_1321del	ENSP00000333938.7:p.Ser440ArgfsTer6
ENST00000342754.5:c.1019_1020del
ENST00000440324.5:c.1278_1279del	ENSP00000411902.1:p.Ser426ArgfsTer6
ENST00000464998.1:n.780_781del
ENST00000480732.2:n.894_895del
NM_001172309.1:c.1128_1129del	NP_001165780.1:p.Ser376ArgfsTer6
NM_144573.3:c.1320_1321del , LRG_442t1:c.1320_1321del	NP_653174.3:p.Ser440ArgfsTer6
XM_005271322.2:c.1320_1321del	XP_005271379.1:p.Ser440ArgfsTer6
XM_005271323.2:c.1278_1279del	XP_005271380.1:p.Ser426ArgfsTer6
XM_005271324.3:c.1128_1129del	XP_005271381.1:p.Ser376ArgfsTer6
XM_005271325.2:c.1251+2412_1251+2413del	XP_005271382.1:n.1251+2412_1251+2413del
XM_005271326.2:c.1086_1087del	XP_005271383.1:p.Ser362ArgfsTer6
XM_005271327.2:c.903_904del	XP_005271384.1:p.Ser301ArgfsTer6
XM_005271322.4:c.1320_1321del	XP_005271379.1:p.Ser440ArgfsTer6
XM_005271323.4:c.1278_1279del	XP_005271380.1:p.Ser426ArgfsTer6
XM_005271324.5:c.1128_1129del	XP_005271381.1:p.Ser376ArgfsTer6
XM_005271325.4:c.1251+2412_1251+2413del	XP_005271382.1:n.1251+2412_1251+2413del
XM_005271326.4:c.1086_1087del	XP_005271383.1:p.Ser362ArgfsTer6
XM_005271327.4:c.903_904del	XP_005271384.1:p.Ser301ArgfsTer6
NM_001172309.2:c.1128_1129del	NP_001165780.1:p.Ser376ArgfsTer6
NM_144573.4:c.1320_1321del MANE Select	NP_653174.3:p.Ser440ArgfsTer6