Canonical Allele Identifier: CA1988802340

Linked Data

dbSNP Id: rs1949241898

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86946304_86946305insCC , CM000673.2:g.86946304_86946305insCC GRCh38
NC_000011.9:g.86657346_86657347insCC , CM000673.1:g.86657346_86657347insCC GRCh37
NC_000011.8:g.86334994_86334995insCC NCBI36
NG_011752.1:g.14088_14089insGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.*4838_*4839insGG (FZD4) MANE Select ENSP00000434034.1:n.*4838_*4839insGG
ENST00000528769.5:n.129-4052_129-4051insCC (PRSS23)
ENST00000531380.1:c.*4838_*4839insGG (FZD4) ENSP00000434034.1:n.*4838_*4839insGG
ENST00000531521.1:n.243-4052_243-4051insCC (PRSS23)
ENST00000532234.5:c.*65-4052_*65-4051insCC (PRSS23) ENSP00000436676.1:n.*65-4052_*65-4051insCC
ENST00000533902.2:c.207-4912_207-4911insCC (PRSS23) ENSP00000437268.1:n.207-4912_207-4911insCC
NM_012193.3:c.*4838_*4839insGG (FZD4) NP_036325.2:n.*4838_*4839insGG
NR_120591.1:n.737-4052_737-4051insCC (PRSS23)
NR_120592.1:n.630-4912_630-4911insCC (PRSS23)
NR_120591.2:n.435-4052_435-4051insCC (PRSS23)
NR_120592.2:n.328-4912_328-4911insCC (PRSS23)
NM_012193.4:c.*4838_*4839insGG (FZD4) MANE Select NP_036325.2:n.*4838_*4839insGG
NR_120591.3:n.435-4052_435-4051insCC (PRSS23)