Canonical Allele Identifier: CA10653938

Gene: ZNF81

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.47918803_47918804del , CM000685.2:g.47918803_47918804del	GRCh38
NC_000023.10:g.47778202_47778203del , CM000685.1:g.47778202_47778203del	GRCh37
NC_000023.9:g.47663146_47663147del	NCBI36
NG_021266.1:g.86902_86903del

Transcript Alleles

HGVS	Amino-acid Change
NM_007137.5:c.*2171_*2172del MANE Select	NP_009068.2:n.*2171_*2172del
ENST00000338637.13:c.*2171_*2172del MANE Select	ENSP00000341151.7:n.*2171_*2172del
NM_001378152.1:c.*2171_*2172del	NP_001365081.1:n.*2171_*2172del
NM_001378153.1:c.*2171_*2172del	NP_001365082.1:n.*2171_*2172del
NM_001378154.1:c.278-5121_278-5120del	NP_001365083.1:n.278-5121_278-5120del
NM_001378155.1:c.278-2505_278-2504del	NP_001365084.1:n.278-2505_278-2504del
NM_007137.3:c.*2171_*2172del	NP_009068.2:n.*2171_*2172del
ENST00000338637.11:c.*2171_*2172del	ENSP00000341151.7:n.*2171_*2172del
ENST00000376950.4:c.277+22863_277+22864del	ENSP00000366149.4:n.277+22863_277+22864del
ENST00000376954.5:c.*2171_*2172del	ENSP00000366153.1:n.*2171_*2172del
ENST00000376954.6:c.*2171_*2172del	ENSP00000366153.1:n.*2171_*2172del
XM_005272600.2:c.*2171_*2172del	XP_005272657.1:n.*2171_*2172del
XM_005272600.3:c.*2171_*2172del	XP_005272657.1:n.*2171_*2172del
XM_011543899.1:c.*2171_*2172del	XP_011542201.1:n.*2171_*2172del
XM_011543899.2:c.*2171_*2172del	XP_011542201.1:n.*2171_*2172del
XM_011543900.1:c.*2171_*2172del	XP_011542202.1:n.*2171_*2172del
XM_011543900.2:c.*2171_*2172del	XP_011542202.1:n.*2171_*2172del
XM_011543901.1:c.*2171_*2172del	XP_011542203.1:n.*2171_*2172del
XM_011543902.1:c.*2171_*2172del	XP_011542204.1:n.*2171_*2172del
XM_017029486.1:c.*2171_*2172del	XP_016884975.1:n.*2171_*2172del
XM_017029487.1:c.*2171_*2172del	XP_016884976.1:n.*2171_*2172del