Canonical Allele Identifier: CA225379999

Linked Data

dbSNP Id: rs1009682639

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951075T>A , CM000673.2:g.86951075T>A GRCh38
NC_000011.9:g.86662117T>A , CM000673.1:g.86662117T>A GRCh37
NC_000011.8:g.86339765T>A NCBI36
NG_011752.1:g.9317A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000531380.2:c.*67A>T (FZD4) MANE Select ENSP00000434034.1:n.*67A>T
ENST00000528769.5:n.273-141T>A (PRSS23)
ENST00000531380.1:c.*67A>T (FZD4) ENSP00000434034.1:n.*67A>T
ENST00000531521.1:n.387-141T>A (PRSS23)
ENST00000532234.5:c.*209-141T>A (PRSS23) ENSP00000436676.1:n.*209-141T>A
ENST00000533902.2:c.207-141T>A (PRSS23) ENSP00000437268.1:n.207-141T>A
NM_012193.3:c.*67A>T (FZD4) NP_036325.2:n.*67A>T
NR_120591.1:n.881-141T>A (PRSS23)
NR_120592.1:n.630-141T>A (PRSS23)
NR_120591.2:n.579-141T>A (PRSS23)
NR_120592.2:n.328-141T>A (PRSS23)
NM_012193.4:c.*67A>T (FZD4) MANE Select NP_036325.2:n.*67A>T
NR_120591.3:n.579-141T>A (PRSS23)