Canonical Allele Identifier: CA2582672905
Gene: ZNF788P HGNC NCBI
ZNF20 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.12114577C>A , CM000681.2:g.12114577C>A GRCh38
NC_000019.9:g.12225392C>A , CM000681.1:g.12225392C>A GRCh37
NC_000019.8:g.12086392C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000430298.6:c.*3273C>A (ZNF788P) ENSP00000391703.1:n.*3273C>A
ENST00000600335.5:c.191+20923G>T (ZNF20) ENSP00000470025.1:n.191+20923G>T
ENST00000601686.1:n.165-21198C>A (ZNF788P)
NR_027049.1:n.3667C>A (ZNF788P)
NM_001348163.1:c.*1182C>A (ZNF788P) NP_001335092.1:n.*1182C>A
NM_001348164.1:c.*1182C>A (ZNF788P) NP_001335093.1:n.*1182C>A
NM_001348165.1:c.*1182C>A (ZNF788P) NP_001335094.1:n.*1182C>A
XM_024451502.1:c.*1182C>A (ZNF788P) XP_024307270.1:n.*1182C>A
NM_001348163.2:c.*1182C>A (ZNF788P) NP_001335092.1:n.*1182C>A
NM_001348164.2:c.*1182C>A (ZNF788P) NP_001335093.1:n.*1182C>A
NM_001348165.2:c.*1182C>A (ZNF788P) NP_001335094.1:n.*1182C>A
NR_171037.1:n.3693C>A (ZNF788P)
NR_171038.1:n.3506C>A (ZNF788P)
NR_171039.1:n.3633C>A (ZNF788P)
NR_171040.1:n.3754C>A (ZNF788P)
NR_171041.1:n.3627C>A (ZNF788P)
NR_171042.1:n.3567C>A (ZNF788P)
NR_171043.1:n.3694C>A (ZNF788P)