Canonical Allele Identifier: CA225380173

Gene: FZD4 PRSS23

Linked Data

• dbSNP Id: rs566786953
• gnomAD v3: 11-86951175-C-G
• gnomAD v4: 11-86951175-C-G
• MyVariant Identifiers: chr11:g.86662217C>G (hg19) ; chr11:g.86951175C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.86951175C>G , CM000673.2:g.86951175C>G	GRCh38
NC_000011.9:g.86662217C>G , CM000673.1:g.86662217C>G	GRCh37
NC_000011.8:g.86339865C>G	NCBI36
NG_011752.1:g.9217G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000531380.2:c.1581G>C (FZD4) MANE Select	ENSP00000434034.1:p.Val527=
ENST00000528769.5:n.273-41C>G (PRSS23)
ENST00000531380.1:c.1581G>C (FZD4)	ENSP00000434034.1:p.Val527=
ENST00000531521.1:n.387-41C>G (PRSS23)
ENST00000532234.5:c.*209-41C>G (PRSS23)	ENSP00000436676.1:n.*209-41C>G
ENST00000533902.2:c.207-41C>G (PRSS23)	ENSP00000437268.1:n.207-41C>G
NM_012193.3:c.1581G>C (FZD4)	NP_036325.2:p.Val527=
NR_120591.1:n.881-41C>G (PRSS23)
NR_120592.1:n.630-41C>G (PRSS23)
NR_120591.2:n.579-41C>G (PRSS23)
NR_120592.2:n.328-41C>G (PRSS23)
NM_012193.4:c.1581G>C (FZD4) MANE Select	NP_036325.2:p.Val527=
NR_120591.3:n.579-41C>G (PRSS23)