Canonical Allele Identifier: CA600757394

Linked Data

dbSNP Id: rs1565395515

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86948076_86948077insTT , CM000673.2:g.86948076_86948077insTT GRCh38
NC_000011.9:g.86659118_86659119insTT , CM000673.1:g.86659118_86659119insTT GRCh37
NC_000011.8:g.86336766_86336767insTT NCBI36
NG_011752.1:g.12315_12316insAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.*3065_*3066insAA (FZD4) MANE Select ENSP00000434034.1:n.*3065_*3066insAA
ENST00000528769.5:n.129-2280_129-2279insTT (PRSS23)
ENST00000531380.1:c.*3065_*3066insAA (FZD4) ENSP00000434034.1:n.*3065_*3066insAA
ENST00000531521.1:n.243-2280_243-2279insTT (PRSS23)
ENST00000532234.5:c.*65-2280_*65-2279insTT (PRSS23) ENSP00000436676.1:n.*65-2280_*65-2279insTT
ENST00000533902.2:c.207-3140_207-3139insTT (PRSS23) ENSP00000437268.1:n.207-3140_207-3139insTT
NM_012193.3:c.*3065_*3066insAA (FZD4) NP_036325.2:n.*3065_*3066insAA
NR_120591.1:n.737-2280_737-2279insTT (PRSS23)
NR_120592.1:n.630-3140_630-3139insTT (PRSS23)
NR_120591.2:n.435-2280_435-2279insTT (PRSS23)
NR_120592.2:n.328-3140_328-3139insTT (PRSS23)
NM_012193.4:c.*3065_*3066insAA (FZD4) MANE Select NP_036325.2:n.*3065_*3066insAA
NR_120591.3:n.435-2280_435-2279insTT (PRSS23)