Canonical Allele Identifier: CA2615460827

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86950748T>G , CM000673.2:g.86950748T>G GRCh38
NC_000011.9:g.86661790T>G , CM000673.1:g.86661790T>G GRCh37
NC_000011.8:g.86339438T>G NCBI36
NG_011752.1:g.9644A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.*394A>C (FZD4) MANE Select ENSP00000434034.1:n.*394A>C
ENST00000528769.5:n.272+249T>G (PRSS23)
ENST00000531380.1:c.*394A>C (FZD4) ENSP00000434034.1:n.*394A>C
ENST00000531521.1:n.386+249T>G (PRSS23)
ENST00000532234.5:c.*208+249T>G (PRSS23) ENSP00000436676.1:n.*208+249T>G
ENST00000533902.2:c.207-468T>G (PRSS23) ENSP00000437268.1:n.207-468T>G
NM_012193.3:c.*394A>C (FZD4) NP_036325.2:n.*394A>C
NR_120591.1:n.880+249T>G (PRSS23)
NR_120592.1:n.630-468T>G (PRSS23)
NR_120591.2:n.578+249T>G (PRSS23)
NR_120592.2:n.328-468T>G (PRSS23)
NM_012193.4:c.*394A>C (FZD4) MANE Select NP_036325.2:n.*394A>C
NR_120591.3:n.578+249T>G (PRSS23)