Canonical Allele Identifier: CA2615460801

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86950714G>T , CM000673.2:g.86950714G>T GRCh38
NC_000011.9:g.86661756G>T , CM000673.1:g.86661756G>T GRCh37
NC_000011.8:g.86339404G>T NCBI36
NG_011752.1:g.9678C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.*428C>A (FZD4) MANE Select ENSP00000434034.1:n.*428C>A
ENST00000528769.5:n.272+215G>T (PRSS23)
ENST00000531380.1:c.*428C>A (FZD4) ENSP00000434034.1:n.*428C>A
ENST00000531521.1:n.386+215G>T (PRSS23)
ENST00000532234.5:c.*208+215G>T (PRSS23) ENSP00000436676.1:n.*208+215G>T
ENST00000533902.2:c.207-502G>T (PRSS23) ENSP00000437268.1:n.207-502G>T
NM_012193.3:c.*428C>A (FZD4) NP_036325.2:n.*428C>A
NR_120591.1:n.880+215G>T (PRSS23)
NR_120592.1:n.630-502G>T (PRSS23)
NR_120591.2:n.578+215G>T (PRSS23)
NR_120592.2:n.328-502G>T (PRSS23)
NM_012193.4:c.*428C>A (FZD4) MANE Select NP_036325.2:n.*428C>A
NR_120591.3:n.578+215G>T (PRSS23)