Canonical Allele Identifier: CA1988808793

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86952054A= , CM000673.2:g.86952054A= GRCh38
NC_000011.9:g.86663096A= , CM000673.1:g.86663096A= GRCh37
NC_000011.8:g.86340744A= NCBI36
NG_011752.1:g.8338T=

Transcript Alleles

HGVS Amino-acid change
ENST00000531380.2:c.702T= (FZD4) MANE Select ENSP00000434034.1:p.Thr234=
ENST00000531380.1:c.702T= (FZD4) ENSP00000434034.1:p.Thr234=
ENST00000532234.5:c.*1047A= (PRSS23) ENSP00000436676.1:n.*1047A=
ENST00000533902.2:c.*769A= (PRSS23) ENSP00000437268.1:n.*769A=
NM_012193.3:c.702T= (FZD4) NP_036325.2:p.Thr234=
NR_120591.1:n.1719A= (PRSS23)
NR_120592.1:n.1468A= (PRSS23)
NR_120591.2:n.1417A= (PRSS23)
NR_120592.2:n.1166A= (PRSS23)
NM_012193.4:c.702T= (FZD4) MANE Select NP_036325.2:p.Thr234=
NR_120591.3:n.1417A= (PRSS23)