Canonical Allele Identifier: CA2241069934

Gene: ZNF469

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88427327_88427329delinsCCT , CM000678.2:g.88427327_88427329delinsCCT	GRCh38
NC_000016.9:g.88493735_88493737delinsCCT , CM000678.1:g.88493735_88493737delinsCCT	GRCh37
NC_000016.8:g.87021236_87021238delinsCCT	NCBI36
NG_012236.2:g.4857_4859delinsCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000565624.3:c.-126-18_-126-16delinsCCT MANE Select	ENSP00000456500.2:n.-126-18_-126-16delinsCCT
XM_011523386.1:c.-126-18_-126-16delinsCCT	XP_011521688.1:n.-126-18_-126-16delinsCCT
XM_011523387.1:c.-126-18_-126-16delinsCCT	XP_011521689.1:n.-126-18_-126-16delinsCCT
XM_011523388.1:c.-126-18_-126-16delinsCCT	XP_011521690.1:n.-126-18_-126-16delinsCCT
XM_017023784.1:c.-144_-142delinsCCT	XP_016879273.1:n.-144_-142delinsCCT
XM_017023785.1:c.-126-18_-126-16delinsCCT	XP_016879274.1:n.-126-18_-126-16delinsCCT
XR_002957934.1:n.250+2635_250+2637delinsAGG
NM_001367624.2:c.-126-18_-126-16delinsCCT MANE Select	NP_001354553.1:n.-126-18_-126-16delinsCCT