Canonical Allele Identifier: CA2634823994
Gene: ZNF469 HGNC NCBI

Linked Data

gnomAD v4: 16-88427386-T-TC
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.88427387dup , CM000678.2:g.88427387dup GRCh38
NC_000016.9:g.88493795dup , CM000678.1:g.88493795dup GRCh37
NC_000016.8:g.87021296dup NCBI36
NG_012236.2:g.4917dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000565624.3:c.-84dup MANE Select ENSP00000456500.2:n.-84dup
XM_011523386.1:c.-84dup XP_011521688.1:n.-84dup
XM_011523387.1:c.-84dup XP_011521689.1:n.-84dup
XM_011523388.1:c.-84dup XP_011521690.1:n.-84dup
XM_017023784.1:c.-84dup XP_016879273.1:n.-84dup
XM_017023785.1:c.-84dup XP_016879274.1:n.-84dup
XR_002957934.1:n.250+2577dup
NM_001367624.2:c.-84dup MANE Select NP_001354553.1:n.-84dup
Search 100 bp 5'
Search 100 bp 3'