Canonical Allele Identifier: CA667276906
Gene: ZNF365 HGNC NCBI

Linked Data

dbSNP Id: rs1309691969
gnomAD v3: 10-62531583-GCAAGACTCCAT-G
gnomAD v4: 10-62531583-GCAAGACTCCAT-G
MyVariant Identifiers: chr10:g.64291343_64291353del (hg19) chr10:g.62531584_62531594del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.62531587_62531597del , CM000672.2:g.62531587_62531597del GRCh38
NC_000010.10:g.64291346_64291356del , CM000672.1:g.64291346_64291356del GRCh37
NC_000010.9:g.63961352_63961362del NCBI36
NG_021209.1:g.162431_162441del

Transcript Alleles

HGVS Amino-acid Change
ENST00000647733.1:c.981+71790_981+71800del ENSP00000502188.1:n.981+71790_981+71800del
ENST00000395251.5:c.-185+10990_-185+11000del ENSP00000378672.1:n.-185+10990_-185+11000del
ENST00000410046.7:c.981+71790_981+71800del ENSP00000387091.3:n.981+71790_981+71800del
NM_199451.2:c.981+71790_981+71800del NP_955523.1:n.981+71790_981+71800del
NM_199452.3:c.-185+10990_-185+11000del NP_955524.3:n.-185+10990_-185+11000del
XM_017015937.2:c.982-12622_982-12612del XP_016871426.1:n.982-12622_982-12612del
NM_199451.3:c.981+71790_981+71800del NP_955523.1:n.981+71790_981+71800del
Search 100 bp 5'
Search 100 bp 3'