Canonical Allele Identifier: CA1988808809

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86952058G= , CM000673.2:g.86952058G= GRCh38
NC_000011.9:g.86663100G= , CM000673.1:g.86663100G= GRCh37
NC_000011.8:g.86340748G= NCBI36
NG_011752.1:g.8334C=

Transcript Alleles

HGVS Amino-acid change
ENST00000531380.2:c.698C= (FZD4) MANE Select ENSP00000434034.1:p.Ser233=
ENST00000531380.1:c.698C= (FZD4) ENSP00000434034.1:p.Ser233=
ENST00000532234.5:c.*1051G= (PRSS23) ENSP00000436676.1:n.*1051G=
ENST00000533902.2:c.*773G= (PRSS23) ENSP00000437268.1:n.*773G=
NM_012193.3:c.698C= (FZD4) NP_036325.2:p.Ser233=
NR_120591.1:n.1723G= (PRSS23)
NR_120592.1:n.1472G= (PRSS23)
NR_120591.2:n.1421G= (PRSS23)
NR_120592.2:n.1170G= (PRSS23)
NM_012193.4:c.698C= (FZD4) MANE Select NP_036325.2:p.Ser233=
NR_120591.3:n.1421G= (PRSS23)