Canonical Allele Identifier: CA1988808063

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951482G= , CM000673.2:g.86951482G= GRCh38
NC_000011.9:g.86662524G= , CM000673.1:g.86662524G= GRCh37
NC_000011.8:g.86340172G= NCBI36
NG_011752.1:g.8910C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.1274C= (FZD4) MANE Select ENSP00000434034.1:p.Thr425=
ENST00000531380.1:c.1274C= (FZD4) ENSP00000434034.1:p.Thr425=
ENST00000531521.1:n.653G= (PRSS23)
ENST00000532234.5:c.*475G= (PRSS23) ENSP00000436676.1:n.*475G=
ENST00000533902.2:c.*197G= (PRSS23) ENSP00000437268.1:n.*197G=
NM_012193.3:c.1274C= (FZD4) NP_036325.2:p.Thr425=
NR_120591.1:n.1147G= (PRSS23)
NR_120592.1:n.896G= (PRSS23)
NR_120591.2:n.845G= (PRSS23)
NR_120592.2:n.594G= (PRSS23)
NM_012193.4:c.1274C= (FZD4) MANE Select NP_036325.2:p.Thr425=
NR_120591.3:n.845G= (PRSS23)