Canonical Allele Identifier: CA681335316

Gene: FZD4 PRSS23

Linked Data

• dbSNP Id: rs1235505189
• MyVariant Identifiers: chr11:g.86657386_86657387insAAG (hg19) ; chr11:g.86946344_86946345insAAG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.86946345_86946347dup , CM000673.2:g.86946345_86946347dup	GRCh38
NC_000011.9:g.86657387_86657389dup , CM000673.1:g.86657387_86657389dup	GRCh37
NC_000011.8:g.86335035_86335037dup	NCBI36
NG_011752.1:g.14045_14047dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000531380.2:c.*4795_*4797dup (FZD4) MANE Select	ENSP00000434034.1:n.*4795_*4797dup
ENST00000528769.5:n.129-4011_129-4009dup (PRSS23)
ENST00000531380.1:c.*4795_*4797dup (FZD4)	ENSP00000434034.1:n.*4795_*4797dup
ENST00000531521.1:n.243-4011_243-4009dup (PRSS23)
ENST00000532234.5:c.*65-4011_*65-4009dup (PRSS23)	ENSP00000436676.1:n.*65-4011_*65-4009dup
ENST00000533902.2:c.207-4871_207-4869dup (PRSS23)	ENSP00000437268.1:n.207-4871_207-4869dup
NM_012193.3:c.*4795_*4797dup (FZD4)	NP_036325.2:n.*4795_*4797dup
NR_120591.1:n.737-4011_737-4009dup (PRSS23)
NR_120592.1:n.630-4871_630-4869dup (PRSS23)
NR_120591.2:n.435-4011_435-4009dup (PRSS23)
NR_120592.2:n.328-4871_328-4869dup (PRSS23)
NM_012193.4:c.*4795_*4797dup (FZD4) MANE Select	NP_036325.2:n.*4795_*4797dup
NR_120591.3:n.435-4011_435-4009dup (PRSS23)