Canonical Allele Identifier: CA2793028850

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86946386_86946387insA , CM000673.2:g.86946386_86946387insA GRCh38
NC_000011.9:g.86657428_86657429insA , CM000673.1:g.86657428_86657429insA GRCh37
NC_000011.8:g.86335076_86335077insA NCBI36
NG_011752.1:g.14005_14006insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.*4755_*4756insT (FZD4) MANE Select ENSP00000434034.1:n.*4755_*4756insT
ENST00000528769.5:n.129-3970_129-3969insA (PRSS23)
ENST00000531380.1:c.*4755_*4756insT (FZD4) ENSP00000434034.1:n.*4755_*4756insT
ENST00000531521.1:n.243-3970_243-3969insA (PRSS23)
ENST00000532234.5:c.*65-3970_*65-3969insA (PRSS23) ENSP00000436676.1:n.*65-3970_*65-3969insA
ENST00000533902.2:c.207-4830_207-4829insA (PRSS23) ENSP00000437268.1:n.207-4830_207-4829insA
NM_012193.3:c.*4755_*4756insT (FZD4) NP_036325.2:n.*4755_*4756insT
NR_120591.1:n.737-3970_737-3969insA (PRSS23)
NR_120592.1:n.630-4830_630-4829insA (PRSS23)
NR_120591.2:n.435-3970_435-3969insA (PRSS23)
NR_120592.2:n.328-4830_328-4829insA (PRSS23)
NM_012193.4:c.*4755_*4756insT (FZD4) MANE Select NP_036325.2:n.*4755_*4756insT
NR_120591.3:n.435-3970_435-3969insA (PRSS23)