Canonical Allele Identifier: CA645125586
Gene: ZIC3 HGNC NCBI

Linked Data

dbSNP Id: rs749955088
gnomAD v2: X-136649009-C-CGCT
gnomAD v3: X-137566850-C-CGCT
gnomAD v4: X-137566850-C-CGCT
MyVariant Identifiers: chrX:g.136649012_136649013insGCT (hg19) chrX:g.136649009_136649010insGCT (hg19) chrX:g.137566850_137566851insGCT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.137566853_137566855dup , CM000685.2:g.137566853_137566855dup GRCh38
NC_000023.10:g.136649012_136649014dup , CM000685.1:g.136649012_136649014dup GRCh37
NC_000023.9:g.136476678_136476680dup NCBI36
NG_008115.1:g.5667_5669dup
NG_008115.2:g.5727_5729dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000287538.10:c.162_164dup MANE Select ENSP00000287538.5:p.Ala55_Phe56insAla
ENST00000287538.9:c.162_164dup ENSP00000287538.5:p.Ala55_Phe56insAla
ENST00000370606.3:c.162_164dup ENSP00000359638.3:p.Ala55_Phe56insAla
NM_003413.3:c.162_164dup NP_003404.1:p.Ala55_Phe56insAla
NM_001330661.1:c.162_164dup NP_001317590.1:p.Ala55_Phe56insAla
NM_003413.4:c.162_164dup MANE Select NP_003404.1:p.Ala55_Phe56insAla
Search 100 bp 5'
Search 100 bp 3'