Canonical Allele Identifier: CA1988803995

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86947827G= , CM000673.2:g.86947827G= GRCh38
NC_000011.9:g.86658869G= , CM000673.1:g.86658869G= GRCh37
NC_000011.8:g.86336517G= NCBI36
NG_011752.1:g.12565C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.*3315C= (FZD4) MANE Select ENSP00000434034.1:n.*3315C=
ENST00000528769.5:n.129-2529G= (PRSS23)
ENST00000531380.1:c.*3315C= (FZD4) ENSP00000434034.1:n.*3315C=
ENST00000531521.1:n.243-2529G= (PRSS23)
ENST00000532234.5:c.*65-2529G= (PRSS23) ENSP00000436676.1:n.*65-2529G=
ENST00000533902.2:c.207-3389G= (PRSS23) ENSP00000437268.1:n.207-3389G=
NM_012193.3:c.*3315C= (FZD4) NP_036325.2:n.*3315C=
NR_120591.1:n.737-2529G= (PRSS23)
NR_120592.1:n.630-3389G= (PRSS23)
NR_120591.2:n.435-2529G= (PRSS23)
NR_120592.2:n.328-3389G= (PRSS23)
NM_012193.4:c.*3315C= (FZD4) MANE Select NP_036325.2:n.*3315C=
NR_120591.3:n.435-2529G= (PRSS23)