Canonical Allele Identifier: CA2600639596

Gene: NEXN

Linked Data

• gnomAD v3: 1-77918036-CAGGTAAGAAGCTTGAGGGGTAAATAGTAAATTAAATTGCAAAATAGAAACATAACCAAGTATCAAACTTTTTTTTCATATATTTTT-C
• gnomAD v4: 1-77918036-CAGGTAAGAAGCTTGAGGGGTAAATAGTAAATTAAATTGCAAAATAGAAACATAACCAAGTATCAAACTTTTTTTTCATATATTTTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77918040_77918125del , CM000663.2:g.77918040_77918125del	GRCh38
NC_000001.10:g.78383725_78383810del , CM000663.1:g.78383725_78383810del	GRCh37
NC_000001.9:g.78156313_78156398del	NCBI36
NG_016625.1:g.34526_34611del , LRG_442:g.34526_34611del

Transcript Alleles

HGVS	Amino-acid change
ENST00000334785.12:c.298+2_299del
ENST00000330010.12:c.106+2_107del
ENST00000334785.11:c.298+2_299del
ENST00000401035.7:c.106+2_107del
ENST00000440324.5:c.298+2_299del
NM_001172309.1:c.106+2_107del
NM_144573.3:c.298+2_299del , LRG_442t1:c.298+2_299del
XM_005271322.2:c.298+2_299del
XM_005271323.2:c.298+2_299del
XM_005271324.3:c.106+2_107del
XM_005271325.2:c.298+2_299del
XM_005271326.2:c.106+2_107del
XM_005271327.2:c.298+2_299del
XM_005271322.4:c.298+2_299del
XM_005271323.4:c.298+2_299del
XM_005271324.5:c.106+2_107del
XM_005271325.4:c.298+2_299del
XM_005271326.4:c.106+2_107del
XM_005271327.4:c.298+2_299del
NM_001172309.2:c.106+2_107del
NM_144573.4:c.298+2_299del