Canonical Allele Identifier: CA2241069901

Gene: ZNF469

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88427284_88427286delinsCCT , CM000678.2:g.88427284_88427286delinsCCT	GRCh38
NC_000016.9:g.88493692_88493694delinsCCT , CM000678.1:g.88493692_88493694delinsCCT	GRCh37
NC_000016.8:g.87021193_87021195delinsCCT	NCBI36
NG_012236.2:g.4814_4816delinsCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000565624.3:c.-126-61_-126-59delinsCCT MANE Select	ENSP00000456500.2:n.-126-61_-126-59delinsCCT
XM_011523386.1:c.-126-61_-126-59delinsCCT	XP_011521688.1:n.-126-61_-126-59delinsCCT
XM_011523387.1:c.-126-61_-126-59delinsCCT	XP_011521689.1:n.-126-61_-126-59delinsCCT
XM_011523388.1:c.-126-61_-126-59delinsCCT	XP_011521690.1:n.-126-61_-126-59delinsCCT
XM_017023784.1:c.-187_-185delinsCCT	XP_016879273.1:n.-187_-185delinsCCT
XM_017023785.1:c.-126-61_-126-59delinsCCT	XP_016879274.1:n.-126-61_-126-59delinsCCT
XR_002957934.1:n.250+2678_250+2680delinsAGG
NM_001367624.2:c.-126-61_-126-59delinsCCT MANE Select	NP_001354553.1:n.-126-61_-126-59delinsCCT