Canonical Allele Identifier: CA681338151

Gene: FZD4 PRSS23

Linked Data

• dbSNP Id: rs1327721568
• gnomAD v3: 11-86951071-TTAG-T
• gnomAD v4: 11-86951071-TTAG-T
• MyVariant Identifiers: chr11:g.86662114_86662116del (hg19) ; chr11:g.86951072_86951074del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.86951075_86951077del , CM000673.2:g.86951075_86951077del	GRCh38
NC_000011.9:g.86662117_86662119del , CM000673.1:g.86662117_86662119del	GRCh37
NC_000011.8:g.86339765_86339767del	NCBI36
NG_011752.1:g.9318_9320del

Transcript Alleles

HGVS	Amino-acid change
ENST00000531380.2:c.*68_*70del (FZD4) MANE Select	ENSP00000434034.1:n.*68_*70del
ENST00000528769.5:n.273-141_273-139del (PRSS23)
ENST00000531380.1:c.*68_*70del (FZD4)	ENSP00000434034.1:n.*68_*70del
ENST00000531521.1:n.387-141_387-139del (PRSS23)
ENST00000532234.5:c.*209-141_*209-139del (PRSS23)	ENSP00000436676.1:n.*209-141_*209-139del
ENST00000533902.2:c.207-141_207-139del (PRSS23)	ENSP00000437268.1:n.207-141_207-139del
NM_012193.3:c.*68_*70del (FZD4)	NP_036325.2:n.*68_*70del
NR_120591.1:n.881-141_881-139del (PRSS23)
NR_120592.1:n.630-141_630-139del (PRSS23)
NR_120591.2:n.579-141_579-139del (PRSS23)
NR_120592.2:n.328-141_328-139del (PRSS23)
NM_012193.4:c.*68_*70del (FZD4) MANE Select	NP_036325.2:n.*68_*70del
NR_120591.3:n.579-141_579-139del (PRSS23)