Canonical Allele Identifier: CA2582672886

Gene: ZNF788P ZNF20

Linked Data

• gnomAD v4: 19-12114544-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12114544C>T , CM000681.2:g.12114544C>T	GRCh38
NC_000019.9:g.12225359C>T , CM000681.1:g.12225359C>T	GRCh37
NC_000019.8:g.12086359C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000430298.6:c.*3240C>T (ZNF788P)	ENSP00000391703.1:n.*3240C>T
ENST00000600335.5:c.191+20956G>A (ZNF20)	ENSP00000470025.1:n.191+20956G>A
ENST00000601686.1:n.165-21231C>T (ZNF788P)
NR_027049.1:n.3634C>T (ZNF788P)
NM_001348163.1:c.*1149C>T (ZNF788P)	NP_001335092.1:n.*1149C>T
NM_001348164.1:c.*1149C>T (ZNF788P)	NP_001335093.1:n.*1149C>T
NM_001348165.1:c.*1149C>T (ZNF788P)	NP_001335094.1:n.*1149C>T
XM_024451502.1:c.*1149C>T (ZNF788P)	XP_024307270.1:n.*1149C>T
NM_001348163.2:c.*1149C>T (ZNF788P)	NP_001335092.1:n.*1149C>T
NM_001348164.2:c.*1149C>T (ZNF788P)	NP_001335093.1:n.*1149C>T
NM_001348165.2:c.*1149C>T (ZNF788P)	NP_001335094.1:n.*1149C>T
NR_171037.1:n.3660C>T (ZNF788P)
NR_171038.1:n.3473C>T (ZNF788P)
NR_171039.1:n.3600C>T (ZNF788P)
NR_171040.1:n.3721C>T (ZNF788P)
NR_171041.1:n.3594C>T (ZNF788P)
NR_171042.1:n.3534C>T (ZNF788P)
NR_171043.1:n.3661C>T (ZNF788P)