Canonical Allele Identifier: CA2499780740

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942079_77942080del , CM000663.2:g.77942079_77942080del	GRCh38
NC_000001.10:g.78407764_78407765del , CM000663.1:g.78407764_78407765del	GRCh37
NC_000001.9:g.78180352_78180353del	NCBI36
NG_016625.1:g.58565_58566del , LRG_442:g.58565_58566del
NG_033243.2:g.42014_42015del

Transcript Alleles

HGVS	Amino-acid change
ENST00000334785.12:c.1530_1531del MANE Select	ENSP00000333938.7:p.Lys510AsnfsTer6
ENST00000330010.12:c.1338_1339del	ENSP00000327363.8:p.Lys446AsnfsTer6
ENST00000334785.11:c.1530_1531del	ENSP00000333938.7:p.Lys510AsnfsTer6
ENST00000342754.5:c.1229_1230del
ENST00000470735.1:n.369_370del
ENST00000480732.2:n.1104_1105del
NM_001172309.1:c.1338_1339del	NP_001165780.1:p.Lys446AsnfsTer6
NM_144573.3:c.1530_1531del , LRG_442t1:c.1530_1531del	NP_653174.3:p.Lys510AsnfsTer6
XM_005271322.2:c.1530_1531del	XP_005271379.1:p.Lys510AsnfsTer6
XM_005271323.2:c.1488_1489del	XP_005271380.1:p.Lys496AsnfsTer6
XM_005271324.3:c.1338_1339del	XP_005271381.1:p.Lys446AsnfsTer6
XM_005271325.2:c.1308_1309del	XP_005271382.1:p.Lys436AsnfsTer6
XM_005271326.2:c.1296_1297del	XP_005271383.1:p.Lys432AsnfsTer6
XM_005271327.2:c.1113_1114del	XP_005271384.1:p.Lys371AsnfsTer6
XM_005271322.4:c.1530_1531del	XP_005271379.1:p.Lys510AsnfsTer6
XM_005271323.4:c.1488_1489del	XP_005271380.1:p.Lys496AsnfsTer6
XM_005271324.5:c.1338_1339del	XP_005271381.1:p.Lys446AsnfsTer6
XM_005271325.4:c.1308_1309del	XP_005271382.1:p.Lys436AsnfsTer6
XM_005271326.4:c.1296_1297del	XP_005271383.1:p.Lys432AsnfsTer6
XM_005271327.4:c.1113_1114del	XP_005271384.1:p.Lys371AsnfsTer6
NM_001172309.2:c.1338_1339del	NP_001165780.1:p.Lys446AsnfsTer6
NM_144573.4:c.1530_1531del MANE Select	NP_653174.3:p.Lys510AsnfsTer6