Canonical Allele Identifier: CA2582672914

Gene: ZNF788P ZNF20

Linked Data

• gnomAD v4: 19-12114599-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12114599G>T , CM000681.2:g.12114599G>T	GRCh38
NC_000019.9:g.12225414G>T , CM000681.1:g.12225414G>T	GRCh37
NC_000019.8:g.12086414G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000430298.6:c.*3295G>T (ZNF788P)	ENSP00000391703.1:n.*3295G>T
ENST00000600335.5:c.191+20901C>A (ZNF20)	ENSP00000470025.1:n.191+20901C>A
ENST00000601686.1:n.165-21176G>T (ZNF788P)
NR_027049.1:n.3689G>T (ZNF788P)
NM_001348163.1:c.*1204G>T (ZNF788P)	NP_001335092.1:n.*1204G>T
NM_001348164.1:c.*1204G>T (ZNF788P)	NP_001335093.1:n.*1204G>T
NM_001348165.1:c.*1204G>T (ZNF788P)	NP_001335094.1:n.*1204G>T
XM_024451502.1:c.*1204G>T (ZNF788P)	XP_024307270.1:n.*1204G>T
NM_001348163.2:c.*1204G>T (ZNF788P)	NP_001335092.1:n.*1204G>T
NM_001348164.2:c.*1204G>T (ZNF788P)	NP_001335093.1:n.*1204G>T
NM_001348165.2:c.*1204G>T (ZNF788P)	NP_001335094.1:n.*1204G>T
NR_171037.1:n.3715G>T (ZNF788P)
NR_171038.1:n.3528G>T (ZNF788P)
NR_171039.1:n.3655G>T (ZNF788P)
NR_171040.1:n.3776G>T (ZNF788P)
NR_171041.1:n.3649G>T (ZNF788P)
NR_171042.1:n.3589G>T (ZNF788P)
NR_171043.1:n.3716G>T (ZNF788P)