Canonical Allele Identifier: CA382014939

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86952086C>T , CM000673.2:g.86952086C>T GRCh38
NC_000011.9:g.86663128C>T , CM000673.1:g.86663128C>T GRCh37
NC_000011.8:g.86340776C>T NCBI36
NG_011752.1:g.8306G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000531380.2:c.670G>A (FZD4) MANE Select ENSP00000434034.1:p.Ala224Thr
ENST00000531380.1:c.670G>A (FZD4) ENSP00000434034.1:p.Ala224Thr
ENST00000532234.5:c.*1079C>T (PRSS23) ENSP00000436676.1:n.*1079C>T
ENST00000533902.2:c.*801C>T (PRSS23) ENSP00000437268.1:n.*801C>T
NM_012193.3:c.670G>A (FZD4) NP_036325.2:p.Ala224Thr
NR_120591.1:n.1751C>T (PRSS23)
NR_120592.1:n.1500C>T (PRSS23)
NR_120591.2:n.1449C>T (PRSS23)
NR_120592.2:n.1198C>T (PRSS23)
NM_012193.4:c.670G>A (FZD4) MANE Select NP_036325.2:p.Ala224Thr
NR_120591.3:n.1449C>T (PRSS23)