Canonical Allele Identifier: CA243945375
Gene: PPP1CC HGNC NCBI

Linked Data

dbSNP Id: rs554557299
gnomAD v2: 12-111155209-CTT-C
gnomAD v3: 12-110717404-CTT-C
gnomAD v4: 12-110717404-CTT-C
MyVariant Identifiers: chr12:g.111155210_111155211del (hg19) chr12:g.111155211_111155213delinsG (hg19) chr12:g.110717405_110717406del (hg38) chr12:g.110717406_110717408delinsG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.110717406_110717407del , CM000674.2:g.110717406_110717407del GRCh38
NC_000012.11:g.111155211_111155212del , CM000674.1:g.111155211_111155212del GRCh37
NC_000012.10:g.109639594_109639595del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011538504.1:c.944-2259_944-2258del XP_011536806.1:n.944-2259_944-2258del
XM_011538505.1:c.943+3699_943+3700del XP_011536807.1:n.943+3699_943+3700del
XM_011538504.3:c.944-2259_944-2258del XP_011536806.1:n.944-2259_944-2258del
XM_011538505.3:c.943+3699_943+3700del XP_011536807.1:n.943+3699_943+3700del
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