Canonical Allele Identifier: CA1988808750

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86952026C= , CM000673.2:g.86952026C= GRCh38
NC_000011.9:g.86663068C= , CM000673.1:g.86663068C= GRCh37
NC_000011.8:g.86340716C= NCBI36
NG_011752.1:g.8366G=

Transcript Alleles

HGVS Amino-acid change
ENST00000531380.2:c.730G= (FZD4) MANE Select ENSP00000434034.1:p.Asp244=
ENST00000531380.1:c.730G= (FZD4) ENSP00000434034.1:p.Asp244=
ENST00000532234.5:c.*1019C= (PRSS23) ENSP00000436676.1:n.*1019C=
ENST00000533902.2:c.*741C= (PRSS23) ENSP00000437268.1:n.*741C=
NM_012193.3:c.730G= (FZD4) NP_036325.2:p.Asp244=
NR_120591.1:n.1691C= (PRSS23)
NR_120592.1:n.1440C= (PRSS23)
NR_120591.2:n.1389C= (PRSS23)
NR_120592.2:n.1138C= (PRSS23)
NM_012193.4:c.730G= (FZD4) MANE Select NP_036325.2:p.Asp244=
NR_120591.3:n.1389C= (PRSS23)