Canonical Allele Identifier: CA382016336

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86952310G>A , CM000673.2:g.86952310G>A GRCh38
NC_000011.9:g.86663352G>A , CM000673.1:g.86663352G>A GRCh37
NC_000011.8:g.86341000G>A NCBI36
NG_011752.1:g.8082C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.446C>T (FZD4) MANE Select ENSP00000434034.1:p.Pro149Leu
ENST00000531380.1:c.446C>T (FZD4) ENSP00000434034.1:p.Pro149Leu
ENST00000532234.5:c.*1303G>A (PRSS23) ENSP00000436676.1:n.*1303G>A
ENST00000533902.2:c.*1025G>A (PRSS23) ENSP00000437268.1:n.*1025G>A
NM_012193.3:c.446C>T (FZD4) NP_036325.2:p.Pro149Leu
NR_120591.1:n.1975G>A (PRSS23)
NR_120592.1:n.1724G>A (PRSS23)
NR_120591.2:n.1673G>A (PRSS23)
NR_120592.2:n.1422G>A (PRSS23)
NM_012193.4:c.446C>T (FZD4) MANE Select NP_036325.2:p.Pro149Leu
NR_120591.3:n.1673G>A (PRSS23)