Canonical Allele Identifier: CA2586966787

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942677_77942678del , CM000663.2:g.77942677_77942678del	GRCh38
NC_000001.10:g.78408362_78408363del , CM000663.1:g.78408362_78408363del	GRCh37
NC_000001.9:g.78180950_78180951del	NCBI36
NG_016625.1:g.59163_59164del , LRG_442:g.59163_59164del
NG_033243.2:g.41418_41419del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1876_1877del MANE Select	ENSP00000333938.7:p.Glu626ArgfsTer6
ENST00000330010.12:c.1684_1685del	ENSP00000327363.8:p.Glu562ArgfsTer6
ENST00000334785.11:c.1876_1877del	ENSP00000333938.7:p.Glu626ArgfsTer6
ENST00000342754.5:c.1575_1576del
ENST00000470735.1:n.715_716del
ENST00000480732.2:n.1450_1451del
NM_001172309.1:c.1684_1685del	NP_001165780.1:p.Glu562ArgfsTer6
NM_144573.3:c.1876_1877del , LRG_442t1:c.1876_1877del	NP_653174.3:p.Glu626ArgfsTer6
XM_005271322.2:c.1876_1877del	XP_005271379.1:p.Glu626ArgfsTer6
XM_005271323.2:c.1834_1835del	XP_005271380.1:p.Glu612ArgfsTer6
XM_005271324.3:c.1684_1685del	XP_005271381.1:p.Glu562ArgfsTer6
XM_005271325.2:c.1654_1655del	XP_005271382.1:p.Glu552ArgfsTer6
XM_005271326.2:c.1642_1643del	XP_005271383.1:p.Glu548ArgfsTer6
XM_005271327.2:c.1459_1460del	XP_005271384.1:p.Glu487ArgfsTer6
XM_005271322.4:c.1876_1877del	XP_005271379.1:p.Glu626ArgfsTer6
XM_005271323.4:c.1834_1835del	XP_005271380.1:p.Glu612ArgfsTer6
XM_005271324.5:c.1684_1685del	XP_005271381.1:p.Glu562ArgfsTer6
XM_005271325.4:c.1654_1655del	XP_005271382.1:p.Glu552ArgfsTer6
XM_005271326.4:c.1642_1643del	XP_005271383.1:p.Glu548ArgfsTer6
XM_005271327.4:c.1459_1460del	XP_005271384.1:p.Glu487ArgfsTer6
NM_001172309.2:c.1684_1685del	NP_001165780.1:p.Glu562ArgfsTer6
NM_144573.4:c.1876_1877del MANE Select	NP_653174.3:p.Glu626ArgfsTer6