Canonical Allele Identifier: CA761931648
Gene: ZNF804A HGNC NCBI

Linked Data

dbSNP Id: rs1306085017
MyVariant Identifiers: chr2:g.185779834_185779835insTCTGTAA (hg19) chr2:g.184915107_184915108insTCTGTAA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.184915107_184915108insTCTGTAA , CM000664.2:g.184915107_184915108insTCTGTAA GRCh38
NC_000002.11:g.185779834_185779835insTCTGTAA , CM000664.1:g.185779834_185779835insTCTGTAA GRCh37
NC_000002.10:g.185488079_185488080insTCTGTAA NCBI36
NG_046950.1:g.321742_321743insTCTGTAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000302277.7:c.256-18496_256-18495insTCTGTAA MANE Select ENSP00000303252.6:n.256-18496_256-18495insTCTGTAA
ENST00000302277.6:c.256-18496_256-18495insTCTGTAA ENSP00000303252.6:n.256-18496_256-18495insTCTGTAA
ENST00000613975.1:c.1-18496_1-18495insTCTGTAA ENSP00000483032.1:n.1-18496_1-18495insTCTGTAA
NM_194250.1:c.256-18496_256-18495insTCTGTAA NP_919226.1:n.256-18496_256-18495insTCTGTAA
NM_194250.2:c.256-18496_256-18495insTCTGTAA MANE Select NP_919226.1:n.256-18496_256-18495insTCTGTAA
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