Canonical Allele Identifier: CA382014795

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86952053C>T , CM000673.2:g.86952053C>T GRCh38
NC_000011.9:g.86663095C>T , CM000673.1:g.86663095C>T GRCh37
NC_000011.8:g.86340743C>T NCBI36
NG_011752.1:g.8339G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000531380.2:c.703G>A (FZD4) MANE Select ENSP00000434034.1:p.Ala235Thr
ENST00000531380.1:c.703G>A (FZD4) ENSP00000434034.1:p.Ala235Thr
ENST00000532234.5:c.*1046C>T (PRSS23) ENSP00000436676.1:n.*1046C>T
ENST00000533902.2:c.*768C>T (PRSS23) ENSP00000437268.1:n.*768C>T
NM_012193.3:c.703G>A (FZD4) NP_036325.2:p.Ala235Thr
NR_120591.1:n.1718C>T (PRSS23)
NR_120592.1:n.1467C>T (PRSS23)
NR_120591.2:n.1416C>T (PRSS23)
NR_120592.2:n.1165C>T (PRSS23)
NM_012193.4:c.703G>A (FZD4) MANE Select NP_036325.2:p.Ala235Thr
NR_120591.3:n.1416C>T (PRSS23)