Canonical Allele Identifier: CA871972341
Gene: ZIC3 HGNC NCBI

Linked Data

dbSNP Id: rs766950526
gnomAD v3: X-137566847-C-CGCCGCT
gnomAD v4: X-137566847-C-CGCCGCT
MyVariant Identifiers: chrX:g.136649006_136649007insGCCGCT (hg19) chrX:g.137566847_137566848insGCCGCT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.137566851_137566856dup , CM000685.2:g.137566851_137566856dup GRCh38
NC_000023.10:g.136649010_136649015dup , CM000685.1:g.136649010_136649015dup GRCh37
NC_000023.9:g.136476676_136476681dup NCBI36
NG_008115.1:g.5665_5670dup
NG_008115.2:g.5725_5730dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000287538.10:c.160_165dup MANE Select ENSP00000287538.5:p.Ala55_Phe56insAlaAla
ENST00000287538.9:c.160_165dup ENSP00000287538.5:p.Ala55_Phe56insAlaAla
ENST00000370606.3:c.160_165dup ENSP00000359638.3:p.Ala55_Phe56insAlaAla
NM_003413.3:c.160_165dup NP_003404.1:p.Ala55_Phe56insAlaAla
NM_001330661.1:c.160_165dup NP_001317590.1:p.Ala55_Phe56insAlaAla
NM_003413.4:c.160_165dup MANE Select NP_003404.1:p.Ala55_Phe56insAlaAla
Search 100 bp 5'
Search 100 bp 3'