Canonical Allele Identifier: CA1988808269

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951636T= , CM000673.2:g.86951636T= GRCh38
NC_000011.9:g.86662678T= , CM000673.1:g.86662678T= GRCh37
NC_000011.8:g.86340326T= NCBI36
NG_011752.1:g.8756A=

Transcript Alleles

HGVS Amino-acid change
ENST00000531380.2:c.1120A= (FZD4) MANE Select ENSP00000434034.1:p.Thr374=
ENST00000531380.1:c.1120A= (FZD4) ENSP00000434034.1:p.Thr374=
ENST00000531521.1:n.807T= (PRSS23)
ENST00000532234.5:c.*629T= (PRSS23) ENSP00000436676.1:n.*629T=
ENST00000533902.2:c.*351T= (PRSS23) ENSP00000437268.1:n.*351T=
NM_012193.3:c.1120A= (FZD4) NP_036325.2:p.Thr374=
NR_120591.1:n.1301T= (PRSS23)
NR_120592.1:n.1050T= (PRSS23)
NR_120591.2:n.999T= (PRSS23)
NR_120592.2:n.748T= (PRSS23)
NM_012193.4:c.1120A= (FZD4) MANE Select NP_036325.2:p.Thr374=
NR_120591.3:n.999T= (PRSS23)