Canonical Allele Identifier: CA225379845

Gene: FZD4 PRSS23

Linked Data

• dbSNP Id: rs935159482
• gnomAD v3: 11-86950795-A-G
• gnomAD v4: 11-86950795-A-G
• MyVariant Identifiers: chr11:g.86661837A>G (hg19) ; chr11:g.86950795A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.86950795A>G , CM000673.2:g.86950795A>G	GRCh38
NC_000011.9:g.86661837A>G , CM000673.1:g.86661837A>G	GRCh37
NC_000011.8:g.86339485A>G	NCBI36
NG_011752.1:g.9597T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000531380.2:c.*347T>C (FZD4) MANE Select	ENSP00000434034.1:n.*347T>C
ENST00000528769.5:n.272+296A>G (PRSS23)
ENST00000531380.1:c.*347T>C (FZD4)	ENSP00000434034.1:n.*347T>C
ENST00000531521.1:n.386+296A>G (PRSS23)
ENST00000532234.5:c.*208+296A>G (PRSS23)	ENSP00000436676.1:n.*208+296A>G
ENST00000533902.2:c.207-421A>G (PRSS23)	ENSP00000437268.1:n.207-421A>G
NM_012193.3:c.*347T>C (FZD4)	NP_036325.2:n.*347T>C
NR_120591.1:n.880+296A>G (PRSS23)
NR_120592.1:n.630-421A>G (PRSS23)
NR_120591.2:n.578+296A>G (PRSS23)
NR_120592.2:n.328-421A>G (PRSS23)
NM_012193.4:c.*347T>C (FZD4) MANE Select	NP_036325.2:n.*347T>C
NR_120591.3:n.578+296A>G (PRSS23)