Canonical Allele Identifier: CA1988807833

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951339T= , CM000673.2:g.86951339T= GRCh38
NC_000011.9:g.86662381T= , CM000673.1:g.86662381T= GRCh37
NC_000011.8:g.86340029T= NCBI36
NG_011752.1:g.9053A=

Transcript Alleles

HGVS Amino-acid change
ENST00000531380.2:c.1417A= (FZD4) MANE Select ENSP00000434034.1:p.Asn473=
ENST00000528769.5:n.396T= (PRSS23)
ENST00000531380.1:c.1417A= (FZD4) ENSP00000434034.1:p.Asn473=
ENST00000531521.1:n.510T= (PRSS23)
ENST00000532234.5:c.*332T= (PRSS23) ENSP00000436676.1:n.*332T=
ENST00000533902.2:c.*54T= (PRSS23) ENSP00000437268.1:n.*54T=
NM_012193.3:c.1417A= (FZD4) NP_036325.2:p.Asn473=
NR_120591.1:n.1004T= (PRSS23)
NR_120592.1:n.753T= (PRSS23)
NR_120591.2:n.702T= (PRSS23)
NR_120592.2:n.451T= (PRSS23)
NM_012193.4:c.1417A= (FZD4) MANE Select NP_036325.2:p.Asn473=
NR_120591.3:n.702T= (PRSS23)