Canonical Allele Identifier: CA1988807283

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951003C= , CM000673.2:g.86951003C= GRCh38
NC_000011.9:g.86662045C= , CM000673.1:g.86662045C= GRCh37
NC_000011.8:g.86339693C= NCBI36
NG_011752.1:g.9389G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.*139G= (FZD4) MANE Select ENSP00000434034.1:n.*139G=
ENST00000528769.5:n.273-213C= (PRSS23)
ENST00000531380.1:c.*139G= (FZD4) ENSP00000434034.1:n.*139G=
ENST00000531521.1:n.387-213C= (PRSS23)
ENST00000532234.5:c.*209-213C= (PRSS23) ENSP00000436676.1:n.*209-213C=
ENST00000533902.2:c.207-213C= (PRSS23) ENSP00000437268.1:n.207-213C=
NM_012193.3:c.*139G= (FZD4) NP_036325.2:n.*139G=
NR_120591.1:n.881-213C= (PRSS23)
NR_120592.1:n.630-213C= (PRSS23)
NR_120591.2:n.579-213C= (PRSS23)
NR_120592.2:n.328-213C= (PRSS23)
NM_012193.4:c.*139G= (FZD4) MANE Select NP_036325.2:n.*139G=
NR_120591.3:n.579-213C= (PRSS23)