Canonical Allele Identifier: CA1988808762

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86952030C= , CM000673.2:g.86952030C= GRCh38
NC_000011.9:g.86663072C= , CM000673.1:g.86663072C= GRCh37
NC_000011.8:g.86340720C= NCBI36
NG_011752.1:g.8362G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.726G= (FZD4) MANE Select ENSP00000434034.1:p.Leu242=
ENST00000531380.1:c.726G= (FZD4) ENSP00000434034.1:p.Leu242=
ENST00000532234.5:c.*1023C= (PRSS23) ENSP00000436676.1:n.*1023C=
ENST00000533902.2:c.*745C= (PRSS23) ENSP00000437268.1:n.*745C=
NM_012193.3:c.726G= (FZD4) NP_036325.2:p.Leu242=
NR_120591.1:n.1695C= (PRSS23)
NR_120592.1:n.1444C= (PRSS23)
NR_120591.2:n.1393C= (PRSS23)
NR_120592.2:n.1142C= (PRSS23)
NM_012193.4:c.726G= (FZD4) MANE Select NP_036325.2:p.Leu242=
NR_120591.3:n.1393C= (PRSS23)