Canonical Allele Identifier: CA225380770

Linked Data

dbSNP Id: rs971044324

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951544C>T , CM000673.2:g.86951544C>T GRCh38
NC_000011.9:g.86662586C>T , CM000673.1:g.86662586C>T GRCh37
NC_000011.8:g.86340234C>T NCBI36
NG_011752.1:g.8848G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.1212G>A (FZD4) MANE Select ENSP00000434034.1:p.Leu404=
ENST00000531380.1:c.1212G>A (FZD4) ENSP00000434034.1:p.Leu404=
ENST00000531521.1:n.715C>T (PRSS23)
ENST00000532234.5:c.*537C>T (PRSS23) ENSP00000436676.1:n.*537C>T
ENST00000533902.2:c.*259C>T (PRSS23) ENSP00000437268.1:n.*259C>T
NM_012193.3:c.1212G>A (FZD4) NP_036325.2:p.Leu404=
NR_120591.1:n.1209C>T (PRSS23)
NR_120592.1:n.958C>T (PRSS23)
NR_120591.2:n.907C>T (PRSS23)
NR_120592.2:n.656C>T (PRSS23)
NM_012193.4:c.1212G>A (FZD4) MANE Select NP_036325.2:p.Leu404=
NR_120591.3:n.907C>T (PRSS23)