Canonical Allele Identifier: CA538374567
Gene: ZNF804A HGNC NCBI

Linked Data

dbSNP Id: rs1263019175

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.184913696_184913697del , CM000664.2:g.184913696_184913697del GRCh38
NC_000002.11:g.185778423_185778424del , CM000664.1:g.185778423_185778424del GRCh37
NC_000002.10:g.185486668_185486669del NCBI36
NG_046950.1:g.320331_320332del

Transcript Alleles

HGVS Amino-acid Change
ENST00000302277.7:c.256-19907_256-19906del MANE Select ENSP00000303252.6:n.256-19907_256-19906del
ENST00000302277.6:c.256-19907_256-19906del ENSP00000303252.6:n.256-19907_256-19906del
ENST00000613975.1:c.1-19907_1-19906del ENSP00000483032.1:n.1-19907_1-19906del
NM_194250.1:c.256-19907_256-19906del NP_919226.1:n.256-19907_256-19906del
NM_194250.2:c.256-19907_256-19906del MANE Select NP_919226.1:n.256-19907_256-19906del