Canonical Allele Identifier: CA1988803992

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86947822C= , CM000673.2:g.86947822C= GRCh38
NC_000011.9:g.86658864C= , CM000673.1:g.86658864C= GRCh37
NC_000011.8:g.86336512C= NCBI36
NG_011752.1:g.12570G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.*3320G= (FZD4) MANE Select ENSP00000434034.1:n.*3320G=
ENST00000528769.5:n.129-2534C= (PRSS23)
ENST00000531380.1:c.*3320G= (FZD4) ENSP00000434034.1:n.*3320G=
ENST00000531521.1:n.243-2534C= (PRSS23)
ENST00000532234.5:c.*65-2534C= (PRSS23) ENSP00000436676.1:n.*65-2534C=
ENST00000533902.2:c.207-3394C= (PRSS23) ENSP00000437268.1:n.207-3394C=
NM_012193.3:c.*3320G= (FZD4) NP_036325.2:n.*3320G=
NR_120591.1:n.737-2534C= (PRSS23)
NR_120592.1:n.630-3394C= (PRSS23)
NR_120591.2:n.435-2534C= (PRSS23)
NR_120592.2:n.328-3394C= (PRSS23)
NM_012193.4:c.*3320G= (FZD4) MANE Select NP_036325.2:n.*3320G=
NR_120591.3:n.435-2534C= (PRSS23)