Canonical Allele Identifier: CA1988809226

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86952335C= , CM000673.2:g.86952335C= GRCh38
NC_000011.9:g.86663377C= , CM000673.1:g.86663377C= GRCh37
NC_000011.8:g.86341025C= NCBI36
NG_011752.1:g.8057G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.421G= (FZD4) MANE Select ENSP00000434034.1:p.Glu141=
ENST00000531380.1:c.421G= (FZD4) ENSP00000434034.1:p.Glu141=
ENST00000532234.5:c.*1328C= (PRSS23) ENSP00000436676.1:n.*1328C=
ENST00000533902.2:c.*1050C= (PRSS23) ENSP00000437268.1:n.*1050C=
NM_012193.3:c.421G= (FZD4) NP_036325.2:p.Glu141=
NR_120591.1:n.2000C= (PRSS23)
NR_120592.1:n.1749C= (PRSS23)
NR_120591.2:n.1698C= (PRSS23)
NR_120592.2:n.1447C= (PRSS23)
NM_012193.4:c.421G= (FZD4) MANE Select NP_036325.2:p.Glu141=
NR_120591.3:n.1698C= (PRSS23)