Canonical Allele Identifier: CA600757220

Gene: FZD4 PRSS23

Linked Data

• dbSNP Id: rs1238599917
• gnomAD v2: 11-86657506-TCAGAAA-T
• MyVariant Identifiers: chr11:g.86657507_86657512del (hg19) ; chr11:g.86946465_86946470del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.86946473_86946478del , CM000673.2:g.86946473_86946478del	GRCh38
NC_000011.9:g.86657515_86657520del , CM000673.1:g.86657515_86657520del	GRCh37
NC_000011.8:g.86335163_86335168del	NCBI36
NG_011752.1:g.13922_13927del

Transcript Alleles

HGVS	Amino-acid change
ENST00000531380.2:c.*4672_*4677del (FZD4) MANE Select	ENSP00000434034.1:n.*4672_*4677del
ENST00000528769.5:n.129-3883_129-3878del (PRSS23)
ENST00000531380.1:c.*4672_*4677del (FZD4)	ENSP00000434034.1:n.*4672_*4677del
ENST00000531521.1:n.243-3883_243-3878del (PRSS23)
ENST00000532234.5:c.*65-3883_*65-3878del (PRSS23)	ENSP00000436676.1:n.*65-3883_*65-3878del
ENST00000533902.2:c.207-4743_207-4738del (PRSS23)	ENSP00000437268.1:n.207-4743_207-4738del
NM_012193.3:c.*4672_*4677del (FZD4)	NP_036325.2:n.*4672_*4677del
NR_120591.1:n.737-3883_737-3878del (PRSS23)
NR_120592.1:n.630-4743_630-4738del (PRSS23)
NR_120591.2:n.435-3883_435-3878del (PRSS23)
NR_120592.2:n.328-4743_328-4738del (PRSS23)
NM_012193.4:c.*4672_*4677del (FZD4) MANE Select	NP_036325.2:n.*4672_*4677del
NR_120591.3:n.435-3883_435-3878del (PRSS23)