Canonical Allele Identifier: CA918887

Gene: NEXN

Linked Data

• dbSNP Id: rs774607878
• ExAC: 1:78401751 CAT / C
• gnomAD v2: 1-78401751-CAT-C
• gnomAD v4: 1-77936066-CAT-C
• MyVariant Identifiers: chr1:g.78401752_78401753del (hg19) ; chr1:g.77936067_77936068del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77936068_77936069del , CM000663.2:g.77936068_77936069del	GRCh38
NC_000001.10:g.78401753_78401754del , CM000663.1:g.78401753_78401754del	GRCh37
NC_000001.9:g.78174341_78174342del	NCBI36
NG_016625.1:g.52554_52555del , LRG_442:g.52554_52555del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1473+24_1473+25del MANE Select	ENSP00000333938.7:n.1473+24_1473+25del
ENST00000330010.12:c.1281+24_1281+25del	ENSP00000327363.8:n.1281+24_1281+25del
ENST00000334785.11:c.1473+24_1473+25del	ENSP00000333938.7:n.1473+24_1473+25del
ENST00000342754.5:c.1172+24_1172+25del
ENST00000480732.2:n.1047+24_1047+25del
NM_001172309.1:c.1281+24_1281+25del	NP_001165780.1:n.1281+24_1281+25del
NM_144573.3:c.1473+24_1473+25del , LRG_442t1:c.1473+24_1473+25del	NP_653174.3:n.1473+24_1473+25del
XM_005271322.2:c.1473+24_1473+25del	XP_005271379.1:n.1473+24_1473+25del
XM_005271323.2:c.1431+24_1431+25del	XP_005271380.1:n.1431+24_1431+25del
XM_005271324.3:c.1281+24_1281+25del	XP_005271381.1:n.1281+24_1281+25del
XM_005271325.2:c.1251+2589_1251+2590del	XP_005271382.1:n.1251+2589_1251+2590del
XM_005271326.2:c.1239+24_1239+25del	XP_005271383.1:n.1239+24_1239+25del
XM_005271327.2:c.1056+24_1056+25del	XP_005271384.1:n.1056+24_1056+25del
XM_005271322.4:c.1473+24_1473+25del	XP_005271379.1:n.1473+24_1473+25del
XM_005271323.4:c.1431+24_1431+25del	XP_005271380.1:n.1431+24_1431+25del
XM_005271324.5:c.1281+24_1281+25del	XP_005271381.1:n.1281+24_1281+25del
XM_005271325.4:c.1251+2589_1251+2590del	XP_005271382.1:n.1251+2589_1251+2590del
XM_005271326.4:c.1239+24_1239+25del	XP_005271383.1:n.1239+24_1239+25del
XM_005271327.4:c.1056+24_1056+25del	XP_005271384.1:n.1056+24_1056+25del
NM_001172309.2:c.1281+24_1281+25del	NP_001165780.1:n.1281+24_1281+25del
NM_144573.4:c.1473+24_1473+25del MANE Select	NP_653174.3:n.1473+24_1473+25del