Canonical Allele Identifier: CA2582672926

Gene: ZNF788P ZNF20

Linked Data

• gnomAD v4: 19-12114627-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12114627G>T , CM000681.2:g.12114627G>T	GRCh38
NC_000019.9:g.12225442G>T , CM000681.1:g.12225442G>T	GRCh37
NC_000019.8:g.12086442G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000430298.6:c.*3323G>T (ZNF788P)	ENSP00000391703.1:n.*3323G>T
ENST00000600335.5:c.191+20873C>A (ZNF20)	ENSP00000470025.1:n.191+20873C>A
ENST00000601686.1:n.165-21148G>T (ZNF788P)
NR_027049.1:n.3717G>T (ZNF788P)
NM_001348163.1:c.*1232G>T (ZNF788P)	NP_001335092.1:n.*1232G>T
NM_001348164.1:c.*1232G>T (ZNF788P)	NP_001335093.1:n.*1232G>T
NM_001348165.1:c.*1232G>T (ZNF788P)	NP_001335094.1:n.*1232G>T
XM_024451502.1:c.*1232G>T (ZNF788P)	XP_024307270.1:n.*1232G>T
NM_001348163.2:c.*1232G>T (ZNF788P)	NP_001335092.1:n.*1232G>T
NM_001348164.2:c.*1232G>T (ZNF788P)	NP_001335093.1:n.*1232G>T
NM_001348165.2:c.*1232G>T (ZNF788P)	NP_001335094.1:n.*1232G>T
NR_171037.1:n.3743G>T (ZNF788P)
NR_171038.1:n.3556G>T (ZNF788P)
NR_171039.1:n.3683G>T (ZNF788P)
NR_171040.1:n.3804G>T (ZNF788P)
NR_171041.1:n.3677G>T (ZNF788P)
NR_171042.1:n.3617G>T (ZNF788P)
NR_171043.1:n.3744G>T (ZNF788P)