Canonical Allele Identifier: CA1988807949

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951374T= , CM000673.2:g.86951374T= GRCh38
NC_000011.9:g.86662416T= , CM000673.1:g.86662416T= GRCh37
NC_000011.8:g.86340064T= NCBI36
NG_011752.1:g.9018A=

Transcript Alleles

HGVS Amino-acid change
ENST00000531380.2:c.1382A= (FZD4) MANE Select ENSP00000434034.1:p.Asn461=
ENST00000528769.5:n.431T= (PRSS23)
ENST00000531380.1:c.1382A= (FZD4) ENSP00000434034.1:p.Asn461=
ENST00000531521.1:n.545T= (PRSS23)
ENST00000532234.5:c.*367T= (PRSS23) ENSP00000436676.1:n.*367T=
ENST00000533902.2:c.*89T= (PRSS23) ENSP00000437268.1:n.*89T=
NM_012193.3:c.1382A= (FZD4) NP_036325.2:p.Asn461=
NR_120591.1:n.1039T= (PRSS23)
NR_120592.1:n.788T= (PRSS23)
NR_120591.2:n.737T= (PRSS23)
NR_120592.2:n.486T= (PRSS23)
NM_012193.4:c.1382A= (FZD4) MANE Select NP_036325.2:p.Asn461=
NR_120591.3:n.737T= (PRSS23)