Canonical Allele Identifier: CA1988808475

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951813C= , CM000673.2:g.86951813C= GRCh38
NC_000011.9:g.86662855C= , CM000673.1:g.86662855C= GRCh37
NC_000011.8:g.86340503C= NCBI36
NG_011752.1:g.8579G=

Transcript Alleles

HGVS Amino-acid change
ENST00000531380.2:c.943G= (FZD4) MANE Select ENSP00000434034.1:p.Ala315=
ENST00000531380.1:c.943G= (FZD4) ENSP00000434034.1:p.Ala315=
ENST00000532234.5:c.*806C= (PRSS23) ENSP00000436676.1:n.*806C=
ENST00000533902.2:c.*528C= (PRSS23) ENSP00000437268.1:n.*528C=
NM_012193.3:c.943G= (FZD4) NP_036325.2:p.Ala315=
NR_120591.1:n.1478C= (PRSS23)
NR_120592.1:n.1227C= (PRSS23)
NR_120591.2:n.1176C= (PRSS23)
NR_120592.2:n.925C= (PRSS23)
NM_012193.4:c.943G= (FZD4) MANE Select NP_036325.2:p.Ala315=
NR_120591.3:n.1176C= (PRSS23)