Canonical Allele Identifier: CA382011360

Gene: FZD4 PRSS23

Linked Data

• dbSNP Id: rs1162487134
• gnomAD v2: 11-86662392-G-A
• gnomAD v4: 11-86951350-G-A
• MyVariant Identifiers: chr11:g.86662392G>A (hg19) ; chr11:g.86951350G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.86951350G>A , CM000673.2:g.86951350G>A	GRCh38
NC_000011.9:g.86662392G>A , CM000673.1:g.86662392G>A	GRCh37
NC_000011.8:g.86340040G>A	NCBI36
NG_011752.1:g.9042C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000531380.2:c.1406C>T (FZD4) MANE Select	ENSP00000434034.1:p.Ala469Val
ENST00000528769.5:n.407G>A (PRSS23)
ENST00000531380.1:c.1406C>T (FZD4)	ENSP00000434034.1:p.Ala469Val
ENST00000531521.1:n.521G>A (PRSS23)
ENST00000532234.5:c.*343G>A (PRSS23)	ENSP00000436676.1:n.*343G>A
ENST00000533902.2:c.*65G>A (PRSS23)	ENSP00000437268.1:n.*65G>A
NM_012193.3:c.1406C>T (FZD4)	NP_036325.2:p.Ala469Val
NR_120591.1:n.1015G>A (PRSS23)
NR_120592.1:n.764G>A (PRSS23)
NR_120591.2:n.713G>A (PRSS23)
NR_120592.2:n.462G>A (PRSS23)
NM_012193.4:c.1406C>T (FZD4) MANE Select	NP_036325.2:p.Ala469Val
NR_120591.3:n.713G>A (PRSS23)