Canonical Allele Identifier: CA2582672904

Gene: ZNF788P ZNF20

Linked Data

• gnomAD v4: 19-12114569-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12114569T>C , CM000681.2:g.12114569T>C	GRCh38
NC_000019.9:g.12225384T>C , CM000681.1:g.12225384T>C	GRCh37
NC_000019.8:g.12086384T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000430298.6:c.*3265T>C (ZNF788P)	ENSP00000391703.1:n.*3265T>C
ENST00000600335.5:c.191+20931A>G (ZNF20)	ENSP00000470025.1:n.191+20931A>G
ENST00000601686.1:n.165-21206T>C (ZNF788P)
NR_027049.1:n.3659T>C (ZNF788P)
NM_001348163.1:c.*1174T>C (ZNF788P)	NP_001335092.1:n.*1174T>C
NM_001348164.1:c.*1174T>C (ZNF788P)	NP_001335093.1:n.*1174T>C
NM_001348165.1:c.*1174T>C (ZNF788P)	NP_001335094.1:n.*1174T>C
XM_024451502.1:c.*1174T>C (ZNF788P)	XP_024307270.1:n.*1174T>C
NM_001348163.2:c.*1174T>C (ZNF788P)	NP_001335092.1:n.*1174T>C
NM_001348164.2:c.*1174T>C (ZNF788P)	NP_001335093.1:n.*1174T>C
NM_001348165.2:c.*1174T>C (ZNF788P)	NP_001335094.1:n.*1174T>C
NR_171037.1:n.3685T>C (ZNF788P)
NR_171038.1:n.3498T>C (ZNF788P)
NR_171039.1:n.3625T>C (ZNF788P)
NR_171040.1:n.3746T>C (ZNF788P)
NR_171041.1:n.3619T>C (ZNF788P)
NR_171042.1:n.3559T>C (ZNF788P)
NR_171043.1:n.3686T>C (ZNF788P)