Canonical Allele Identifier: CA2793028142

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86946433_86946434insACAG , CM000673.2:g.86946433_86946434insACAG GRCh38
NC_000011.9:g.86657475_86657476insACAG , CM000673.1:g.86657475_86657476insACAG GRCh37
NC_000011.8:g.86335123_86335124insACAG NCBI36
NG_011752.1:g.13958_13959insCTGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.*4708_*4709insCTGT (FZD4) MANE Select ENSP00000434034.1:n.*4708_*4709insCTGT
ENST00000528769.5:n.129-3923_129-3922insACAG (PRSS23)
ENST00000531380.1:c.*4708_*4709insCTGT (FZD4) ENSP00000434034.1:n.*4708_*4709insCTGT
ENST00000531521.1:n.243-3923_243-3922insACAG (PRSS23)
ENST00000532234.5:c.*65-3923_*65-3922insACAG (PRSS23) ENSP00000436676.1:n.*65-3923_*65-3922insACAG
ENST00000533902.2:c.207-4783_207-4782insACAG (PRSS23) ENSP00000437268.1:n.207-4783_207-4782insACAG
NM_012193.3:c.*4708_*4709insCTGT (FZD4) NP_036325.2:n.*4708_*4709insCTGT
NR_120591.1:n.737-3923_737-3922insACAG (PRSS23)
NR_120592.1:n.630-4783_630-4782insACAG (PRSS23)
NR_120591.2:n.435-3923_435-3922insACAG (PRSS23)
NR_120592.2:n.328-4783_328-4782insACAG (PRSS23)
NM_012193.4:c.*4708_*4709insCTGT (FZD4) MANE Select NP_036325.2:n.*4708_*4709insCTGT
NR_120591.3:n.435-3923_435-3922insACAG (PRSS23)