Canonical Allele Identifier: CA2323251752

Gene: ZNF788P ZNF20

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12114557T= , CM000681.2:g.12114557T=	GRCh38
NC_000019.9:g.12225372T= , CM000681.1:g.12225372T=	GRCh37
NC_000019.8:g.12086372T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001348163.1:c.*1162T= (ZNF788P)	NP_001335092.1:n.*1162T=
NM_001348163.2:c.*1162T= (ZNF788P)	NP_001335092.1:n.*1162T=
NM_001348164.1:c.*1162T= (ZNF788P)	NP_001335093.1:n.*1162T=
NM_001348164.2:c.*1162T= (ZNF788P)	NP_001335093.1:n.*1162T=
NM_001348165.1:c.*1162T= (ZNF788P)	NP_001335094.1:n.*1162T=
NM_001348165.2:c.*1162T= (ZNF788P)	NP_001335094.1:n.*1162T=
NR_027049.1:n.3647T= (ZNF788P)
NR_171037.1:n.3673T= (ZNF788P)
NR_171038.1:n.3486T= (ZNF788P)
NR_171039.1:n.3613T= (ZNF788P)
NR_171040.1:n.3734T= (ZNF788P)
NR_171041.1:n.3607T= (ZNF788P)
NR_171042.1:n.3547T= (ZNF788P)
NR_171043.1:n.3674T= (ZNF788P)
ENST00000430298.6:c.*3253T= (ZNF788P)	ENSP00000391703.1:n.*3253T=
ENST00000600335.5:c.191+20943A= (ZNF20)	ENSP00000470025.1:n.191+20943A=
ENST00000601686.1:n.165-21218T= (ZNF788P)
XM_024451502.1:c.*1162T= (ZNF788P)	XP_024307270.1:n.*1162T=