Canonical Allele Identifier: CA1988807999

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951425T= , CM000673.2:g.86951425T= GRCh38
NC_000011.9:g.86662467T= , CM000673.1:g.86662467T= GRCh37
NC_000011.8:g.86340115T= NCBI36
NG_011752.1:g.8967A=

Transcript Alleles

HGVS Amino-acid change
ENST00000531380.2:c.1331A= (FZD4) MANE Select ENSP00000434034.1:p.Tyr444=
ENST00000531380.1:c.1331A= (FZD4) ENSP00000434034.1:p.Tyr444=
ENST00000531521.1:n.596T= (PRSS23)
ENST00000532234.5:c.*418T= (PRSS23) ENSP00000436676.1:n.*418T=
ENST00000533902.2:c.*140T= (PRSS23) ENSP00000437268.1:n.*140T=
NM_012193.3:c.1331A= (FZD4) NP_036325.2:p.Tyr444=
NR_120591.1:n.1090T= (PRSS23)
NR_120592.1:n.839T= (PRSS23)
NR_120591.2:n.788T= (PRSS23)
NR_120592.2:n.537T= (PRSS23)
NM_012193.4:c.1331A= (FZD4) MANE Select NP_036325.2:p.Tyr444=
NR_120591.3:n.788T= (PRSS23)