Canonical Allele Identifier: CA10651931

Gene: ZNF81

Linked Data

• ClinVar Variation Id: 368430
• ClinVar RCV Id: RCV000407404
• dbSNP Id: rs1057515915
• gnomAD v4: X-47920031-T-A
• MyVariant Identifiers: chrX:g.47779430T>A (hg19) ; chrX:g.47920031T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.47920031T>A , CM000685.2:g.47920031T>A	GRCh38
NC_000023.10:g.47779430T>A , CM000685.1:g.47779430T>A	GRCh37
NC_000023.9:g.47664374T>A	NCBI36
NG_021266.1:g.88130T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338637.13:c.*3399T>A MANE Select	ENSP00000341151.7:n.*3399T>A
ENST00000376954.6:c.*3399T>A	ENSP00000366153.1:n.*3399T>A
ENST00000338637.11:c.*3399T>A	ENSP00000341151.7:n.*3399T>A
ENST00000376950.4:c.277+24091T>A	ENSP00000366149.4:n.277+24091T>A
ENST00000376954.5:c.*3399T>A	ENSP00000366153.1:n.*3399T>A
NM_007137.3:c.*3399T>A	NP_009068.2:n.*3399T>A
XM_005272600.2:c.*3399T>A	XP_005272657.1:n.*3399T>A
XM_011543899.1:c.*3399T>A	XP_011542201.1:n.*3399T>A
XM_011543900.1:c.*3399T>A	XP_011542202.1:n.*3399T>A
XM_011543901.1:c.*3399T>A	XP_011542203.1:n.*3399T>A
XM_011543902.1:c.*3399T>A	XP_011542204.1:n.*3399T>A
XM_005272600.3:c.*3399T>A	XP_005272657.1:n.*3399T>A
XM_011543899.2:c.*3399T>A	XP_011542201.1:n.*3399T>A
XM_011543900.2:c.*3399T>A	XP_011542202.1:n.*3399T>A
XM_017029486.1:c.*3399T>A	XP_016884975.1:n.*3399T>A
XM_017029487.1:c.*3399T>A	XP_016884976.1:n.*3399T>A
NM_001378152.1:c.*3399T>A	NP_001365081.1:n.*3399T>A
NM_001378153.1:c.*3399T>A	NP_001365082.1:n.*3399T>A
NM_001378154.1:c.278-3893T>A	NP_001365083.1:n.278-3893T>A
NM_001378155.1:c.278-1277T>A	NP_001365084.1:n.278-1277T>A
NM_007137.5:c.*3399T>A MANE Select	NP_009068.2:n.*3399T>A