Canonical Allele Identifier: CA1988807691

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951250G= , CM000673.2:g.86951250G= GRCh38
NC_000011.9:g.86662292G= , CM000673.1:g.86662292G= GRCh37
NC_000011.8:g.86339940G= NCBI36
NG_011752.1:g.9142C=

Transcript Alleles

HGVS Amino-acid change
ENST00000531380.2:c.1506C= (FZD4) MANE Select ENSP00000434034.1:p.His502=
ENST00000528769.5:n.307G= (PRSS23)
ENST00000531380.1:c.1506C= (FZD4) ENSP00000434034.1:p.His502=
ENST00000531521.1:n.421G= (PRSS23)
ENST00000532234.5:c.*243G= (PRSS23) ENSP00000436676.1:n.*243G=
ENST00000533902.2:c.241G= (PRSS23) ENSP00000437268.1:p.Val81=
NM_012193.3:c.1506C= (FZD4) NP_036325.2:p.His502=
NR_120591.1:n.915G= (PRSS23)
NR_120592.1:n.664G= (PRSS23)
NR_120591.2:n.613G= (PRSS23)
NR_120592.2:n.362G= (PRSS23)
NM_012193.4:c.1506C= (FZD4) MANE Select NP_036325.2:p.His502=
NR_120591.3:n.613G= (PRSS23)