Canonical Allele Identifier: CA1988809181

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86952292T= , CM000673.2:g.86952292T= GRCh38
NC_000011.9:g.86663334T= , CM000673.1:g.86663334T= GRCh37
NC_000011.8:g.86340982T= NCBI36
NG_011752.1:g.8100A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.464A= (FZD4) MANE Select ENSP00000434034.1:p.Asn155=
ENST00000531380.1:c.464A= (FZD4) ENSP00000434034.1:p.Asn155=
ENST00000532234.5:c.*1285T= (PRSS23) ENSP00000436676.1:n.*1285T=
ENST00000533902.2:c.*1007T= (PRSS23) ENSP00000437268.1:n.*1007T=
NM_012193.3:c.464A= (FZD4) NP_036325.2:p.Asn155=
NR_120591.1:n.1957T= (PRSS23)
NR_120592.1:n.1706T= (PRSS23)
NR_120591.2:n.1655T= (PRSS23)
NR_120592.2:n.1404T= (PRSS23)
NM_012193.4:c.464A= (FZD4) MANE Select NP_036325.2:p.Asn155=
NR_120591.3:n.1655T= (PRSS23)