Canonical Allele Identifier: CA382014785

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86952050A>G , CM000673.2:g.86952050A>G GRCh38
NC_000011.9:g.86663092A>G , CM000673.1:g.86663092A>G GRCh37
NC_000011.8:g.86340740A>G NCBI36
NG_011752.1:g.8342T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000531380.2:c.706T>C (FZD4) MANE Select ENSP00000434034.1:p.Phe236Leu
ENST00000531380.1:c.706T>C (FZD4) ENSP00000434034.1:p.Phe236Leu
ENST00000532234.5:c.*1043A>G (PRSS23) ENSP00000436676.1:n.*1043A>G
ENST00000533902.2:c.*765A>G (PRSS23) ENSP00000437268.1:n.*765A>G
NM_012193.3:c.706T>C (FZD4) NP_036325.2:p.Phe236Leu
NR_120591.1:n.1715A>G (PRSS23)
NR_120592.1:n.1464A>G (PRSS23)
NR_120591.2:n.1413A>G (PRSS23)
NR_120592.2:n.1162A>G (PRSS23)
NM_012193.4:c.706T>C (FZD4) MANE Select NP_036325.2:p.Phe236Leu
NR_120591.3:n.1413A>G (PRSS23)