Canonical Allele Identifier: CA2793028841

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86950725_86950726insA , CM000673.2:g.86950725_86950726insA GRCh38
NC_000011.9:g.86661767_86661768insA , CM000673.1:g.86661767_86661768insA GRCh37
NC_000011.8:g.86339415_86339416insA NCBI36
NG_011752.1:g.9666_9667insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.*416_*417insT (FZD4) MANE Select ENSP00000434034.1:n.*416_*417insT
ENST00000528769.5:n.272+226_272+227insA (PRSS23)
ENST00000531380.1:c.*416_*417insT (FZD4) ENSP00000434034.1:n.*416_*417insT
ENST00000531521.1:n.386+226_386+227insA (PRSS23)
ENST00000532234.5:c.*208+226_*208+227insA (PRSS23) ENSP00000436676.1:n.*208+226_*208+227insA
ENST00000533902.2:c.207-491_207-490insA (PRSS23) ENSP00000437268.1:n.207-491_207-490insA
NM_012193.3:c.*416_*417insT (FZD4) NP_036325.2:n.*416_*417insT
NR_120591.1:n.880+226_880+227insA (PRSS23)
NR_120592.1:n.630-491_630-490insA (PRSS23)
NR_120591.2:n.578+226_578+227insA (PRSS23)
NR_120592.2:n.328-491_328-490insA (PRSS23)
NM_012193.4:c.*416_*417insT (FZD4) MANE Select NP_036325.2:n.*416_*417insT
NR_120591.3:n.578+226_578+227insA (PRSS23)