Canonical Allele Identifier: CA681335434

Gene: FZD4 PRSS23

Linked Data

• dbSNP Id: rs1449972400
• gnomAD v3: 11-86946480-GCTA-G
• gnomAD v4: 11-86946480-GCTA-G
• MyVariant Identifiers: chr11:g.86657523_86657525del (hg19) ; chr11:g.86946481_86946483del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.86946484_86946486del , CM000673.2:g.86946484_86946486del	GRCh38
NC_000011.9:g.86657526_86657528del , CM000673.1:g.86657526_86657528del	GRCh37
NC_000011.8:g.86335174_86335176del	NCBI36
NG_011752.1:g.13909_13911del

Transcript Alleles

HGVS	Amino-acid change
ENST00000531380.2:c.*4659_*4661del (FZD4) MANE Select	ENSP00000434034.1:n.*4659_*4661del
ENST00000528769.5:n.129-3872_129-3870del (PRSS23)
ENST00000531380.1:c.*4659_*4661del (FZD4)	ENSP00000434034.1:n.*4659_*4661del
ENST00000531521.1:n.243-3872_243-3870del (PRSS23)
ENST00000532234.5:c.*65-3872_*65-3870del (PRSS23)	ENSP00000436676.1:n.*65-3872_*65-3870del
ENST00000533902.2:c.207-4732_207-4730del (PRSS23)	ENSP00000437268.1:n.207-4732_207-4730del
NM_012193.3:c.*4659_*4661del (FZD4)	NP_036325.2:n.*4659_*4661del
NR_120591.1:n.737-3872_737-3870del (PRSS23)
NR_120592.1:n.630-4732_630-4730del (PRSS23)
NR_120591.2:n.435-3872_435-3870del (PRSS23)
NR_120592.2:n.328-4732_328-4730del (PRSS23)
NM_012193.4:c.*4659_*4661del (FZD4) MANE Select	NP_036325.2:n.*4659_*4661del
NR_120591.3:n.435-3872_435-3870del (PRSS23)