Canonical Allele Identifier: CA1313504172
Gene: ZNF804A HGNC NCBI

Linked Data

dbSNP Id: rs1685423155

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.184915110_184915111insAAAAA , CM000664.2:g.184915110_184915111insAAAAA GRCh38
NC_000002.11:g.185779837_185779838insAAAAA , CM000664.1:g.185779837_185779838insAAAAA GRCh37
NC_000002.10:g.185488082_185488083insAAAAA NCBI36
NG_046950.1:g.321745_321746insAAAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000302277.7:c.256-18493_256-18492insAAAAA MANE Select ENSP00000303252.6:n.256-18493_256-18492insAAAAA
ENST00000302277.6:c.256-18493_256-18492insAAAAA ENSP00000303252.6:n.256-18493_256-18492insAAAAA
ENST00000613975.1:c.1-18493_1-18492insAAAAA ENSP00000483032.1:n.1-18493_1-18492insAAAAA
NM_194250.1:c.256-18493_256-18492insAAAAA NP_919226.1:n.256-18493_256-18492insAAAAA
NM_194250.2:c.256-18493_256-18492insAAAAA MANE Select NP_919226.1:n.256-18493_256-18492insAAAAA