Canonical Allele Identifier: CA10640371

Gene: FZD4 PRSS23

Linked Data

• ClinVar Variation Id: 306332
• ClinVar RCV Id: RCV000375879
• dbSNP Id: rs61903831
• gnomAD v2: 11-86657409-G-A
• gnomAD v3: 11-86946367-G-A
• gnomAD v4: 11-86946367-G-A
• MyVariant Identifiers: chr11:g.86657409G>A (hg19) ; chr11:g.86946367G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.86946367G>A , CM000673.2:g.86946367G>A	GRCh38
NC_000011.9:g.86657409G>A , CM000673.1:g.86657409G>A	GRCh37
NC_000011.8:g.86335057G>A	NCBI36
NG_011752.1:g.14025C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000531380.2:c.*4775C>T (FZD4) MANE Select	ENSP00000434034.1:n.*4775C>T
ENST00000528769.5:n.129-3989G>A (PRSS23)
ENST00000531380.1:c.*4775C>T (FZD4)	ENSP00000434034.1:n.*4775C>T
ENST00000531521.1:n.243-3989G>A (PRSS23)
ENST00000532234.5:c.*65-3989G>A (PRSS23)	ENSP00000436676.1:n.*65-3989G>A
ENST00000533902.2:c.207-4849G>A (PRSS23)	ENSP00000437268.1:n.207-4849G>A
NM_012193.3:c.*4775C>T (FZD4)	NP_036325.2:n.*4775C>T
NR_120591.1:n.737-3989G>A (PRSS23)
NR_120592.1:n.630-4849G>A (PRSS23)
NR_120591.2:n.435-3989G>A (PRSS23)
NR_120592.2:n.328-4849G>A (PRSS23)
NM_012193.4:c.*4775C>T (FZD4) MANE Select	NP_036325.2:n.*4775C>T
NR_120591.3:n.435-3989G>A (PRSS23)