Canonical Allele Identifier: CA2573131973

Gene: NEXN

Linked Data

• ClinVar Variation Id: 1461682
• ClinVar RCV Id: RCV001983393 ; RCV002223331
• dbSNP Id: rs2102147202

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77933480del , CM000663.2:g.77933480del	GRCh38
NC_000001.10:g.78399165del , CM000663.1:g.78399165del	GRCh37
NC_000001.9:g.78171753del	NCBI36
NG_016625.1:g.49966del , LRG_442:g.49966del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1251+1del
ENST00000330010.12:c.1059+1del
ENST00000334785.11:c.1251+1del
ENST00000342754.5:c.950+1del
ENST00000440324.5:c.1209+1del
ENST00000464998.1:n.711+1del
ENST00000480732.2:n.825+1del
NM_001172309.1:c.1059+1del
NM_144573.3:c.1251+1del , LRG_442t1:c.1251+1del
XM_005271322.2:c.1251+1del
XM_005271323.2:c.1209+1del
XM_005271324.3:c.1059+1del
XM_005271325.2:c.1251+1del
XM_005271326.2:c.1017+1del
XM_005271327.2:c.834+1del
XM_005271322.4:c.1251+1del
XM_005271323.4:c.1209+1del
XM_005271324.5:c.1059+1del
XM_005271325.4:c.1251+1del
XM_005271326.4:c.1017+1del
XM_005271327.4:c.834+1del
NM_001172309.2:c.1059+1del
NM_144573.4:c.1251+1del