Canonical Allele Identifier: CA1988808174

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951585C= , CM000673.2:g.86951585C= GRCh38
NC_000011.9:g.86662627C= , CM000673.1:g.86662627C= GRCh37
NC_000011.8:g.86340275C= NCBI36
NG_011752.1:g.8807G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.1171G= (FZD4) MANE Select ENSP00000434034.1:p.Val391=
ENST00000531380.1:c.1171G= (FZD4) ENSP00000434034.1:p.Val391=
ENST00000531521.1:n.756C= (PRSS23)
ENST00000532234.5:c.*578C= (PRSS23) ENSP00000436676.1:n.*578C=
ENST00000533902.2:c.*300C= (PRSS23) ENSP00000437268.1:n.*300C=
NM_012193.3:c.1171G= (FZD4) NP_036325.2:p.Val391=
NR_120591.1:n.1250C= (PRSS23)
NR_120592.1:n.999C= (PRSS23)
NR_120591.2:n.948C= (PRSS23)
NR_120592.2:n.697C= (PRSS23)
NM_012193.4:c.1171G= (FZD4) MANE Select NP_036325.2:p.Val391=
NR_120591.3:n.948C= (PRSS23)