Canonical Allele Identifier: CA382011520

Gene: FZD4 PRSS23

Linked Data

• dbSNP Id: rs1482420806
• gnomAD v2: 11-86662434-T-C
• gnomAD v4: 11-86951392-T-C
• MyVariant Identifiers: chr11:g.86662434T>C (hg19) ; chr11:g.86951392T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.86951392T>C , CM000673.2:g.86951392T>C	GRCh38
NC_000011.9:g.86662434T>C , CM000673.1:g.86662434T>C	GRCh37
NC_000011.8:g.86340082T>C	NCBI36
NG_011752.1:g.9000A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000531380.2:c.1364A>G (FZD4) MANE Select	ENSP00000434034.1:p.Tyr455Cys
ENST00000528769.5:n.449T>C (PRSS23)
ENST00000531380.1:c.1364A>G (FZD4)	ENSP00000434034.1:p.Tyr455Cys
ENST00000531521.1:n.563T>C (PRSS23)
ENST00000532234.5:c.*385T>C (PRSS23)	ENSP00000436676.1:n.*385T>C
ENST00000533902.2:c.*107T>C (PRSS23)	ENSP00000437268.1:n.*107T>C
NM_012193.3:c.1364A>G (FZD4)	NP_036325.2:p.Tyr455Cys
NR_120591.1:n.1057T>C (PRSS23)
NR_120592.1:n.806T>C (PRSS23)
NR_120591.2:n.755T>C (PRSS23)
NR_120592.2:n.504T>C (PRSS23)
NM_012193.4:c.1364A>G (FZD4) MANE Select	NP_036325.2:p.Tyr455Cys
NR_120591.3:n.755T>C (PRSS23)