Canonical Allele Identifier: CA1988808788

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86952046G= , CM000673.2:g.86952046G= GRCh38
NC_000011.9:g.86663088G= , CM000673.1:g.86663088G= GRCh37
NC_000011.8:g.86340736G= NCBI36
NG_011752.1:g.8346C=

Transcript Alleles

HGVS Amino-acid change
ENST00000531380.2:c.710C= (FZD4) MANE Select ENSP00000434034.1:p.Thr237=
ENST00000531380.1:c.710C= (FZD4) ENSP00000434034.1:p.Thr237=
ENST00000532234.5:c.*1039G= (PRSS23) ENSP00000436676.1:n.*1039G=
ENST00000533902.2:c.*761G= (PRSS23) ENSP00000437268.1:n.*761G=
NM_012193.3:c.710C= (FZD4) NP_036325.2:p.Thr237=
NR_120591.1:n.1711G= (PRSS23)
NR_120592.1:n.1460G= (PRSS23)
NR_120591.2:n.1409G= (PRSS23)
NR_120592.2:n.1158G= (PRSS23)
NM_012193.4:c.710C= (FZD4) MANE Select NP_036325.2:p.Thr237=
NR_120591.3:n.1409G= (PRSS23)