Canonical Allele Identifier: CA382010757

Gene: FZD4 PRSS23

Linked Data

• dbSNP Id: rs1311319825
• gnomAD v2: 11-86662192-C-T
• gnomAD v4: 11-86951150-C-T
• MyVariant Identifiers: chr11:g.86662192C>T (hg19) ; chr11:g.86951150C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.86951150C>T , CM000673.2:g.86951150C>T	GRCh38
NC_000011.9:g.86662192C>T , CM000673.1:g.86662192C>T	GRCh37
NC_000011.8:g.86339840C>T	NCBI36
NG_011752.1:g.9242G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000531380.2:c.1606G>A (FZD4) MANE Select	ENSP00000434034.1:p.Val536Met
ENST00000528769.5:n.273-66C>T (PRSS23)
ENST00000531380.1:c.1606G>A (FZD4)	ENSP00000434034.1:p.Val536Met
ENST00000531521.1:n.387-66C>T (PRSS23)
ENST00000532234.5:c.*209-66C>T (PRSS23)	ENSP00000436676.1:n.*209-66C>T
ENST00000533902.2:c.207-66C>T (PRSS23)	ENSP00000437268.1:n.207-66C>T
NM_012193.3:c.1606G>A (FZD4)	NP_036325.2:p.Val536Met
NR_120591.1:n.881-66C>T (PRSS23)
NR_120592.1:n.630-66C>T (PRSS23)
NR_120591.2:n.579-66C>T (PRSS23)
NR_120592.2:n.328-66C>T (PRSS23)
NM_012193.4:c.1606G>A (FZD4) MANE Select	NP_036325.2:p.Val536Met
NR_120591.3:n.579-66C>T (PRSS23)