Canonical Allele Identifier: CA1988809221

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86952333C= , CM000673.2:g.86952333C= GRCh38
NC_000011.9:g.86663375C= , CM000673.1:g.86663375C= GRCh37
NC_000011.8:g.86341023C= NCBI36
NG_011752.1:g.8059G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.423G= (FZD4) MANE Select ENSP00000434034.1:p.Glu141=
ENST00000531380.1:c.423G= (FZD4) ENSP00000434034.1:p.Glu141=
ENST00000532234.5:c.*1326C= (PRSS23) ENSP00000436676.1:n.*1326C=
ENST00000533902.2:c.*1048C= (PRSS23) ENSP00000437268.1:n.*1048C=
NM_012193.3:c.423G= (FZD4) NP_036325.2:p.Glu141=
NR_120591.1:n.1998C= (PRSS23)
NR_120592.1:n.1747C= (PRSS23)
NR_120591.2:n.1696C= (PRSS23)
NR_120592.2:n.1445C= (PRSS23)
NM_012193.4:c.423G= (FZD4) MANE Select NP_036325.2:p.Glu141=
NR_120591.3:n.1696C= (PRSS23)