Canonical Allele Identifier: CA2580616331

Gene: ZNFX1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.49270191_49270192del , CM000682.2:g.49270191_49270192del	GRCh38
NC_000020.10:g.47886728_47886729del , CM000682.1:g.47886728_47886729del	GRCh37
NC_000020.9:g.47320135_47320136del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_021035.3:c.1623_1624del MANE Select	NP_066363.1:p.His542CysfsTer?
ENST00000396105.6:c.1623_1624del MANE Select	ENSP00000379412.1:p.His542CysfsTer?
NM_021035.2:c.1623_1624del	NP_066363.1:p.His542CysfsTer?
ENST00000371744.5:c.1623_1624del	ENSP00000360809.1:p.His542CysfsTer?
ENST00000371752.5:c.1623_1624del	ENSP00000360817.1:p.His542CysfsTer?
ENST00000371754.8:c.1623_1624del	ENSP00000360819.4:p.His542CysfsTer?
ENST00000396105.5:c.1623_1624del	ENSP00000379412.1:p.His542CysfsTer?
ENST00000455070.1:c.1035_1036del	ENSP00000413800.1:p.His346CysfsTer?
XM_006723836.1:c.1623_1624del	XP_006723899.1:p.His542CysfsTer?
XM_011528924.1:c.1623_1624del	XP_011527226.1:p.His542CysfsTer?
XM_011528924.2:c.1623_1624del	XP_011527226.1:p.His542CysfsTer?
XM_017027971.1:c.-613_-612del	XP_016883460.1:n.-613_-612del