Canonical Allele Identifier: CA524231116

Gene: NEXN

Linked Data

• dbSNP Id: rs1194846625
• gnomAD v2: 1-78399145-T-TGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGG
• MyVariant Identifiers: chr1:g.78399145_78399146insGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGG (hg19) ; chr1:g.77933460_77933461insGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77933461_77933462insGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGG , CM000663.2:g.77933461_77933462insGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGG	GRCh38
NC_000001.10:g.78399146_78399147insGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGG , CM000663.1:g.78399146_78399147insGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGG	GRCh37
NC_000001.9:g.78171734_78171735insGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGG	NCBI36
NG_016625.1:g.49947_49948insGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGG , LRG_442:g.49947_49948insGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1233_1234insGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGG
ENST00000330010.12:c.1041_1042insGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGG
ENST00000334785.11:c.1233_1234insGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGG
ENST00000342754.5:c.932_933insGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGG
ENST00000440324.5:c.1191_1192insGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGG
ENST00000464998.1:n.693_694insGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGG
ENST00000480732.2:n.807_808insGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGG
NM_001172309.1:c.1041_1042insGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGG
NM_144573.3:c.1233_1234insGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGG , LRG_442t1:c.1233_1234insGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGG
XM_005271322.2:c.1233_1234insGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGG
XM_005271323.2:c.1191_1192insGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGG
XM_005271324.3:c.1041_1042insGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGG
XM_005271325.2:c.1233_1234insGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGG
XM_005271326.2:c.999_1000insGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGG
XM_005271327.2:c.816_817insGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGG
XM_005271322.4:c.1233_1234insGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGG
XM_005271323.4:c.1191_1192insGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGG
XM_005271324.5:c.1041_1042insGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGG
XM_005271325.4:c.1233_1234insGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGG
XM_005271326.4:c.999_1000insGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGG
XM_005271327.4:c.816_817insGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGG
NM_001172309.2:c.1041_1042insGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGG
NM_144573.4:c.1233_1234insGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGG