Canonical Allele Identifier: CA1988807500

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951162C= , CM000673.2:g.86951162C= GRCh38
NC_000011.9:g.86662204C= , CM000673.1:g.86662204C= GRCh37
NC_000011.8:g.86339852C= NCBI36
NG_011752.1:g.9230G=

Transcript Alleles

HGVS Amino-acid change
ENST00000531380.2:c.1594G= (FZD4) MANE Select ENSP00000434034.1:p.Gly532=
ENST00000528769.5:n.273-54C= (PRSS23)
ENST00000531380.1:c.1594G= (FZD4) ENSP00000434034.1:p.Gly532=
ENST00000531521.1:n.387-54C= (PRSS23)
ENST00000532234.5:c.*209-54C= (PRSS23) ENSP00000436676.1:n.*209-54C=
ENST00000533902.2:c.207-54C= (PRSS23) ENSP00000437268.1:n.207-54C=
NM_012193.3:c.1594G= (FZD4) NP_036325.2:p.Gly532=
NR_120591.1:n.881-54C= (PRSS23)
NR_120592.1:n.630-54C= (PRSS23)
NR_120591.2:n.579-54C= (PRSS23)
NR_120592.2:n.328-54C= (PRSS23)
NM_012193.4:c.1594G= (FZD4) MANE Select NP_036325.2:p.Gly532=
NR_120591.3:n.579-54C= (PRSS23)