Canonical Allele Identifier: CA2808056690
Gene: ZNF469 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.88437184_88437185insACCCAA , CM000678.2:g.88437184_88437185insACCCAA GRCh38
NC_000016.9:g.88503592_88503593insACCCAA , CM000678.1:g.88503592_88503593insACCCAA GRCh37
NC_000016.8:g.87031093_87031094insACCCAA NCBI36
NG_012236.2:g.14714_14715insACCCAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000565624.3:c.9714_9715insACCCAA MANE Select ENSP00000456500.2:p.His3238_His3239insThrGln
ENST00000437464.1:c.9630_9631insACCCAA ENSP00000402343.1:p.His3210_His3211insThrGln
ENST00000565624.1:c.9714_9715insACCCAA ENSP00000456500.1:p.His3238_His3239insThrGln
NM_001127464.2:c.9630_9631insACCCAA NP_001120936.2:p.His3210_His3211insThrGln
XM_011523386.1:c.9714_9715insACCCAA XP_011521688.1:p.His3238_His3239insThrGln
XM_011523387.1:c.9714_9715insACCCAA XP_011521689.1:p.His3238_His3239insThrGln
XM_011523388.1:c.9714_9715insACCCAA XP_011521690.1:p.His3238_His3239insThrGln
XM_017023784.1:c.9714_9715insACCCAA XP_016879273.1:p.His3238_His3239insThrGln
XM_017023785.1:c.9714_9715insACCCAA XP_016879274.1:p.His3238_His3239insThrGln
NM_001367624.1:c.9714_9715insACCCAA NP_001354553.1:p.His3238_His3239insThrGln
NM_001367624.2:c.9714_9715insACCCAA MANE Select NP_001354553.1:p.His3238_His3239insThrGln