Canonical Allele Identifier: CA225379841

Gene: FZD4 PRSS23

Linked Data

• dbSNP Id: rs902636342
• gnomAD v2: 11-86661812-C-G
• gnomAD v3: 11-86950770-C-G
• gnomAD v4: 11-86950770-C-G
• MyVariant Identifiers: chr11:g.86661812C>G (hg19) ; chr11:g.86950770C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.86950770C>G , CM000673.2:g.86950770C>G	GRCh38
NC_000011.9:g.86661812C>G , CM000673.1:g.86661812C>G	GRCh37
NC_000011.8:g.86339460C>G	NCBI36
NG_011752.1:g.9622G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000531380.2:c.*372G>C (FZD4) MANE Select	ENSP00000434034.1:n.*372G>C
ENST00000528769.5:n.272+271C>G (PRSS23)
ENST00000531380.1:c.*372G>C (FZD4)	ENSP00000434034.1:n.*372G>C
ENST00000531521.1:n.386+271C>G (PRSS23)
ENST00000532234.5:c.*208+271C>G (PRSS23)	ENSP00000436676.1:n.*208+271C>G
ENST00000533902.2:c.207-446C>G (PRSS23)	ENSP00000437268.1:n.207-446C>G
NM_012193.3:c.*372G>C (FZD4)	NP_036325.2:n.*372G>C
NR_120591.1:n.880+271C>G (PRSS23)
NR_120592.1:n.630-446C>G (PRSS23)
NR_120591.2:n.578+271C>G (PRSS23)
NR_120592.2:n.328-446C>G (PRSS23)
NM_012193.4:c.*372G>C (FZD4) MANE Select	NP_036325.2:n.*372G>C
NR_120591.3:n.578+271C>G (PRSS23)