Canonical Allele Identifier: CA208592211
Gene: ZNF365 HGNC NCBI

Linked Data

dbSNP Id: rs148479830
gnomAD v2: 10-64288396-A-AG
gnomAD v3: 10-62528637-A-AG
gnomAD v4: 10-62528637-A-AG
MyVariant Identifiers: chr10:g.64288397_64288398insG (hg19) chr10:g.64288396_64288397insG (hg19) chr10:g.62528638_62528639insG (hg38) chr10:g.62528637_62528638insG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.62528638dup , CM000672.2:g.62528638dup GRCh38
NC_000010.10:g.64288397dup , CM000672.1:g.64288397dup GRCh37
NC_000010.9:g.63958403dup NCBI36
NG_021209.1:g.159482dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000647733.1:c.981+68841dup ENSP00000502188.1:n.981+68841dup
ENST00000395251.5:c.-185+8041dup ENSP00000378672.1:n.-185+8041dup
ENST00000410046.7:c.981+68841dup ENSP00000387091.3:n.981+68841dup
NM_199451.2:c.981+68841dup NP_955523.1:n.981+68841dup
NM_199452.3:c.-185+8041dup NP_955524.3:n.-185+8041dup
XM_017015937.2:c.982-15571dup XP_016871426.1:n.982-15571dup
NM_199451.3:c.981+68841dup NP_955523.1:n.981+68841dup
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