Canonical Allele Identifier: CA382016319

Linked Data

dbSNP Id: rs1350373174

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86952308G>A , CM000673.2:g.86952308G>A GRCh38
NC_000011.9:g.86663350G>A , CM000673.1:g.86663350G>A GRCh37
NC_000011.8:g.86340998G>A NCBI36
NG_011752.1:g.8084C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.448C>T (FZD4) MANE Select ENSP00000434034.1:p.Pro150Ser
ENST00000531380.1:c.448C>T (FZD4) ENSP00000434034.1:p.Pro150Ser
ENST00000532234.5:c.*1301G>A (PRSS23) ENSP00000436676.1:n.*1301G>A
ENST00000533902.2:c.*1023G>A (PRSS23) ENSP00000437268.1:n.*1023G>A
NM_012193.3:c.448C>T (FZD4) NP_036325.2:p.Pro150Ser
NR_120591.1:n.1973G>A (PRSS23)
NR_120592.1:n.1722G>A (PRSS23)
NR_120591.2:n.1671G>A (PRSS23)
NR_120592.2:n.1420G>A (PRSS23)
NM_012193.4:c.448C>T (FZD4) MANE Select NP_036325.2:p.Pro150Ser
NR_120591.3:n.1671G>A (PRSS23)