Canonical Allele Identifier: CA918894

Gene: NEXN

Linked Data

• dbSNP Id: rs767863275
• ExAC: 1:78401771 GATA / G
• gnomAD v2: 1-78401771-GATA-G
• gnomAD v3: 1-77936086-GATA-G
• gnomAD v4: 1-77936086-GATA-G
• MyVariant Identifiers: chr1:g.78401772_78401774del (hg19) ; chr1:g.77936087_77936089del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77936091_77936093del , CM000663.2:g.77936091_77936093del	GRCh38
NC_000001.10:g.78401776_78401778del , CM000663.1:g.78401776_78401778del	GRCh37
NC_000001.9:g.78174364_78174366del	NCBI36
NG_016625.1:g.52577_52579del , LRG_442:g.52577_52579del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1473+47_1473+49del MANE Select	ENSP00000333938.7:n.1473+47_1473+49del
ENST00000330010.12:c.1281+47_1281+49del	ENSP00000327363.8:n.1281+47_1281+49del
ENST00000334785.11:c.1473+47_1473+49del	ENSP00000333938.7:n.1473+47_1473+49del
ENST00000342754.5:c.1172+47_1172+49del
ENST00000480732.2:n.1047+47_1047+49del
NM_001172309.1:c.1281+47_1281+49del	NP_001165780.1:n.1281+47_1281+49del
NM_144573.3:c.1473+47_1473+49del , LRG_442t1:c.1473+47_1473+49del	NP_653174.3:n.1473+47_1473+49del
XM_005271322.2:c.1473+47_1473+49del	XP_005271379.1:n.1473+47_1473+49del
XM_005271323.2:c.1431+47_1431+49del	XP_005271380.1:n.1431+47_1431+49del
XM_005271324.3:c.1281+47_1281+49del	XP_005271381.1:n.1281+47_1281+49del
XM_005271325.2:c.1251+2612_1251+2614del	XP_005271382.1:n.1251+2612_1251+2614del
XM_005271326.2:c.1239+47_1239+49del	XP_005271383.1:n.1239+47_1239+49del
XM_005271327.2:c.1056+47_1056+49del	XP_005271384.1:n.1056+47_1056+49del
XM_005271322.4:c.1473+47_1473+49del	XP_005271379.1:n.1473+47_1473+49del
XM_005271323.4:c.1431+47_1431+49del	XP_005271380.1:n.1431+47_1431+49del
XM_005271324.5:c.1281+47_1281+49del	XP_005271381.1:n.1281+47_1281+49del
XM_005271325.4:c.1251+2612_1251+2614del	XP_005271382.1:n.1251+2612_1251+2614del
XM_005271326.4:c.1239+47_1239+49del	XP_005271383.1:n.1239+47_1239+49del
XM_005271327.4:c.1056+47_1056+49del	XP_005271384.1:n.1056+47_1056+49del
NM_001172309.2:c.1281+47_1281+49del	NP_001165780.1:n.1281+47_1281+49del
NM_144573.4:c.1473+47_1473+49del MANE Select	NP_653174.3:n.1473+47_1473+49del