Canonical Allele Identifier: CA681335444

Gene: FZD4 PRSS23

Linked Data

• dbSNP Id: rs1224877953
• gnomAD v4: 11-86946485-T-C
• MyVariant Identifiers: chr11:g.86657527T>C (hg19) ; chr11:g.86946485T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.86946485T>C , CM000673.2:g.86946485T>C	GRCh38
NC_000011.9:g.86657527T>C , CM000673.1:g.86657527T>C	GRCh37
NC_000011.8:g.86335175T>C	NCBI36
NG_011752.1:g.13907A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000531380.2:c.*4657A>G (FZD4) MANE Select	ENSP00000434034.1:n.*4657A>G
ENST00000528769.5:n.129-3871T>C (PRSS23)
ENST00000531380.1:c.*4657A>G (FZD4)	ENSP00000434034.1:n.*4657A>G
ENST00000531521.1:n.243-3871T>C (PRSS23)
ENST00000532234.5:c.*65-3871T>C (PRSS23)	ENSP00000436676.1:n.*65-3871T>C
ENST00000533902.2:c.207-4731T>C (PRSS23)	ENSP00000437268.1:n.207-4731T>C
NM_012193.3:c.*4657A>G (FZD4)	NP_036325.2:n.*4657A>G
NR_120591.1:n.737-3871T>C (PRSS23)
NR_120592.1:n.630-4731T>C (PRSS23)
NR_120591.2:n.435-3871T>C (PRSS23)
NR_120592.2:n.328-4731T>C (PRSS23)
NM_012193.4:c.*4657A>G (FZD4) MANE Select	NP_036325.2:n.*4657A>G
NR_120591.3:n.435-3871T>C (PRSS23)