Canonical Allele Identifier: CA382016014

Linked Data

dbSNP Id: rs1949300846

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86952269C>T , CM000673.2:g.86952269C>T GRCh38
NC_000011.9:g.86663311C>T , CM000673.1:g.86663311C>T GRCh37
NC_000011.8:g.86340959C>T NCBI36
NG_011752.1:g.8123G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000531380.2:c.487G>A (FZD4) MANE Select ENSP00000434034.1:p.Gly163Ser
ENST00000531380.1:c.487G>A (FZD4) ENSP00000434034.1:p.Gly163Ser
ENST00000532234.5:c.*1262C>T (PRSS23) ENSP00000436676.1:n.*1262C>T
ENST00000533902.2:c.*984C>T (PRSS23) ENSP00000437268.1:n.*984C>T
NM_012193.3:c.487G>A (FZD4) NP_036325.2:p.Gly163Ser
NR_120591.1:n.1934C>T (PRSS23)
NR_120592.1:n.1683C>T (PRSS23)
NR_120591.2:n.1632C>T (PRSS23)
NR_120592.2:n.1381C>T (PRSS23)
NM_012193.4:c.487G>A (FZD4) MANE Select NP_036325.2:p.Gly163Ser
NR_120591.3:n.1632C>T (PRSS23)