Canonical Allele Identifier: CA418709420

Gene: NEXN

Linked Data

• COSMIC: COSM1639975
• MyVariant Identifiers: chr1:g.78401614del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77935934del , CM000663.2:g.77935934del	GRCh38
NC_000001.10:g.78401619del , CM000663.1:g.78401619del	GRCh37
NC_000001.9:g.78174207del	NCBI36
NG_016625.1:g.52420del , LRG_442:g.52420del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1363del MANE Select	ENSP00000333938.7:p.Ile455LeufsTer13
ENST00000330010.12:c.1171del	ENSP00000327363.8:p.Ile391LeufsTer13
ENST00000334785.11:c.1363del	ENSP00000333938.7:p.Ile455LeufsTer13
ENST00000342754.5:c.1062del
ENST00000464998.1:n.823del
ENST00000480732.2:n.937del
NM_001172309.1:c.1171del	NP_001165780.1:p.Ile391LeufsTer13
NM_144573.3:c.1363del , LRG_442t1:c.1363del	NP_653174.3:p.Ile455LeufsTer13
XM_005271322.2:c.1363del	XP_005271379.1:p.Ile455LeufsTer13
XM_005271323.2:c.1321del	XP_005271380.1:p.Ile441LeufsTer13
XM_005271324.3:c.1171del	XP_005271381.1:p.Ile391LeufsTer13
XM_005271325.2:c.1251+2455del	XP_005271382.1:n.1251+2455del
XM_005271326.2:c.1129del	XP_005271383.1:p.Ile377LeufsTer13
XM_005271327.2:c.946del	XP_005271384.1:p.Ile316LeufsTer13
XM_005271322.4:c.1363del	XP_005271379.1:p.Ile455LeufsTer13
XM_005271323.4:c.1321del	XP_005271380.1:p.Ile441LeufsTer13
XM_005271324.5:c.1171del	XP_005271381.1:p.Ile391LeufsTer13
XM_005271325.4:c.1251+2455del	XP_005271382.1:n.1251+2455del
XM_005271326.4:c.1129del	XP_005271383.1:p.Ile377LeufsTer13
XM_005271327.4:c.946del	XP_005271384.1:p.Ile316LeufsTer13
NM_001172309.2:c.1171del	NP_001165780.1:p.Ile391LeufsTer13
NM_144573.4:c.1363del MANE Select	NP_653174.3:p.Ile455LeufsTer13