Canonical Allele Identifier: CA1988807020

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86950726T= , CM000673.2:g.86950726T= GRCh38
NC_000011.9:g.86661768T= , CM000673.1:g.86661768T= GRCh37
NC_000011.8:g.86339416T= NCBI36
NG_011752.1:g.9666A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.*416A= (FZD4) MANE Select ENSP00000434034.1:n.*416A=
ENST00000528769.5:n.272+227T= (PRSS23)
ENST00000531380.1:c.*416A= (FZD4) ENSP00000434034.1:n.*416A=
ENST00000531521.1:n.386+227T= (PRSS23)
ENST00000532234.5:c.*208+227T= (PRSS23) ENSP00000436676.1:n.*208+227T=
ENST00000533902.2:c.207-490T= (PRSS23) ENSP00000437268.1:n.207-490T=
NM_012193.3:c.*416A= (FZD4) NP_036325.2:n.*416A=
NR_120591.1:n.880+227T= (PRSS23)
NR_120592.1:n.630-490T= (PRSS23)
NR_120591.2:n.578+227T= (PRSS23)
NR_120592.2:n.328-490T= (PRSS23)
NM_012193.4:c.*416A= (FZD4) MANE Select NP_036325.2:n.*416A=
NR_120591.3:n.578+227T= (PRSS23)