Canonical Allele Identifier: CA2323251809

Gene: ZNF788P ZNF20

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12114667C= , CM000681.2:g.12114667C=	GRCh38
NC_000019.9:g.12225482C= , CM000681.1:g.12225482C=	GRCh37
NC_000019.8:g.12086482C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000430298.6:c.*3363C= (ZNF788P)	ENSP00000391703.1:n.*3363C=
ENST00000600335.5:c.191+20833G= (ZNF20)	ENSP00000470025.1:n.191+20833G=
ENST00000601686.1:n.165-21108C= (ZNF788P)
NR_027049.1:n.3757C= (ZNF788P)
NM_001348163.1:c.*1272C= (ZNF788P)	NP_001335092.1:n.*1272C=
NM_001348164.1:c.*1272C= (ZNF788P)	NP_001335093.1:n.*1272C=
NM_001348165.1:c.*1272C= (ZNF788P)	NP_001335094.1:n.*1272C=
XM_024451502.1:c.*1272C= (ZNF788P)	XP_024307270.1:n.*1272C=
NM_001348163.2:c.*1272C= (ZNF788P)	NP_001335092.1:n.*1272C=
NM_001348164.2:c.*1272C= (ZNF788P)	NP_001335093.1:n.*1272C=
NM_001348165.2:c.*1272C= (ZNF788P)	NP_001335094.1:n.*1272C=
NR_171037.1:n.3783C= (ZNF788P)
NR_171038.1:n.3596C= (ZNF788P)
NR_171039.1:n.3723C= (ZNF788P)
NR_171040.1:n.3844C= (ZNF788P)
NR_171041.1:n.3717C= (ZNF788P)
NR_171042.1:n.3657C= (ZNF788P)
NR_171043.1:n.3784C= (ZNF788P)