Canonical Allele Identifier: CA1988808189

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951590C= , CM000673.2:g.86951590C= GRCh38
NC_000011.9:g.86662632C= , CM000673.1:g.86662632C= GRCh37
NC_000011.8:g.86340280C= NCBI36
NG_011752.1:g.8802G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.1166G= (FZD4) MANE Select ENSP00000434034.1:p.Gly389=
ENST00000531380.1:c.1166G= (FZD4) ENSP00000434034.1:p.Gly389=
ENST00000531521.1:n.761C= (PRSS23)
ENST00000532234.5:c.*583C= (PRSS23) ENSP00000436676.1:n.*583C=
ENST00000533902.2:c.*305C= (PRSS23) ENSP00000437268.1:n.*305C=
NM_012193.3:c.1166G= (FZD4) NP_036325.2:p.Gly389=
NR_120591.1:n.1255C= (PRSS23)
NR_120592.1:n.1004C= (PRSS23)
NR_120591.2:n.953C= (PRSS23)
NR_120592.2:n.702C= (PRSS23)
NM_012193.4:c.1166G= (FZD4) MANE Select NP_036325.2:p.Gly389=
NR_120591.3:n.953C= (PRSS23)