Canonical Allele Identifier: CA1988807013

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86950722C= , CM000673.2:g.86950722C= GRCh38
NC_000011.9:g.86661764C= , CM000673.1:g.86661764C= GRCh37
NC_000011.8:g.86339412C= NCBI36
NG_011752.1:g.9670G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.*420G= (FZD4) MANE Select ENSP00000434034.1:n.*420G=
ENST00000528769.5:n.272+223C= (PRSS23)
ENST00000531380.1:c.*420G= (FZD4) ENSP00000434034.1:n.*420G=
ENST00000531521.1:n.386+223C= (PRSS23)
ENST00000532234.5:c.*208+223C= (PRSS23) ENSP00000436676.1:n.*208+223C=
ENST00000533902.2:c.207-494C= (PRSS23) ENSP00000437268.1:n.207-494C=
NM_012193.3:c.*420G= (FZD4) NP_036325.2:n.*420G=
NR_120591.1:n.880+223C= (PRSS23)
NR_120592.1:n.630-494C= (PRSS23)
NR_120591.2:n.578+223C= (PRSS23)
NR_120592.2:n.328-494C= (PRSS23)
NM_012193.4:c.*420G= (FZD4) MANE Select NP_036325.2:n.*420G=
NR_120591.3:n.578+223C= (PRSS23)