Canonical Allele Identifier: CA1988807682

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951248G= , CM000673.2:g.86951248G= GRCh38
NC_000011.9:g.86662290G= , CM000673.1:g.86662290G= GRCh37
NC_000011.8:g.86339938G= NCBI36
NG_011752.1:g.9144C=

Transcript Alleles

HGVS Amino-acid change
ENST00000531380.2:c.1508C= (FZD4) MANE Select ENSP00000434034.1:p.Thr503=
ENST00000528769.5:n.305G= (PRSS23)
ENST00000531380.1:c.1508C= (FZD4) ENSP00000434034.1:p.Thr503=
ENST00000531521.1:n.419G= (PRSS23)
ENST00000532234.5:c.*241G= (PRSS23) ENSP00000436676.1:n.*241G=
ENST00000533902.2:c.239G= (PRSS23) ENSP00000437268.1:p.Arg80=
NM_012193.3:c.1508C= (FZD4) NP_036325.2:p.Thr503=
NR_120591.1:n.913G= (PRSS23)
NR_120592.1:n.662G= (PRSS23)
NR_120591.2:n.611G= (PRSS23)
NR_120592.2:n.360G= (PRSS23)
NM_012193.4:c.1508C= (FZD4) MANE Select NP_036325.2:p.Thr503=
NR_120591.3:n.611G= (PRSS23)