Canonical Allele Identifier: CA382014911

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86952079C>T , CM000673.2:g.86952079C>T GRCh38
NC_000011.9:g.86663121C>T , CM000673.1:g.86663121C>T GRCh37
NC_000011.8:g.86340769C>T NCBI36
NG_011752.1:g.8313G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000531380.2:c.677G>A (FZD4) MANE Select ENSP00000434034.1:p.Trp226Ter
ENST00000531380.1:c.677G>A (FZD4) ENSP00000434034.1:p.Trp226Ter
ENST00000532234.5:c.*1072C>T (PRSS23) ENSP00000436676.1:n.*1072C>T
ENST00000533902.2:c.*794C>T (PRSS23) ENSP00000437268.1:n.*794C>T
NM_012193.3:c.677G>A (FZD4) NP_036325.2:p.Trp226Ter
NR_120591.1:n.1744C>T (PRSS23)
NR_120592.1:n.1493C>T (PRSS23)
NR_120591.2:n.1442C>T (PRSS23)
NR_120592.2:n.1191C>T (PRSS23)
NM_012193.4:c.677G>A (FZD4) MANE Select NP_036325.2:p.Trp226Ter
NR_120591.3:n.1442C>T (PRSS23)