Canonical Allele Identifier: CA1988809135

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86952254G= , CM000673.2:g.86952254G= GRCh38
NC_000011.9:g.86663296G= , CM000673.1:g.86663296G= GRCh37
NC_000011.8:g.86340944G= NCBI36
NG_011752.1:g.8138C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.502C= (FZD4) MANE Select ENSP00000434034.1:p.Pro168=
ENST00000531380.1:c.502C= (FZD4) ENSP00000434034.1:p.Pro168=
ENST00000532234.5:c.*1247G= (PRSS23) ENSP00000436676.1:n.*1247G=
ENST00000533902.2:c.*969G= (PRSS23) ENSP00000437268.1:n.*969G=
NM_012193.3:c.502C= (FZD4) NP_036325.2:p.Pro168=
NR_120591.1:n.1919G= (PRSS23)
NR_120592.1:n.1668G= (PRSS23)
NR_120591.2:n.1617G= (PRSS23)
NR_120592.2:n.1366G= (PRSS23)
NM_012193.4:c.502C= (FZD4) MANE Select NP_036325.2:p.Pro168=
NR_120591.3:n.1617G= (PRSS23)