Canonical Allele Identifier: CA681337999

Linked Data

dbSNP Id: rs1414407404

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86950819G>C , CM000673.2:g.86950819G>C GRCh38
NC_000011.9:g.86661861G>C , CM000673.1:g.86661861G>C GRCh37
NC_000011.8:g.86339509G>C NCBI36
NG_011752.1:g.9573C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.*323C>G (FZD4) MANE Select ENSP00000434034.1:n.*323C>G
ENST00000528769.5:n.272+320G>C (PRSS23)
ENST00000531380.1:c.*323C>G (FZD4) ENSP00000434034.1:n.*323C>G
ENST00000531521.1:n.386+320G>C (PRSS23)
ENST00000532234.5:c.*208+320G>C (PRSS23) ENSP00000436676.1:n.*208+320G>C
ENST00000533902.2:c.207-397G>C (PRSS23) ENSP00000437268.1:n.207-397G>C
NM_012193.3:c.*323C>G (FZD4) NP_036325.2:n.*323C>G
NR_120591.1:n.880+320G>C (PRSS23)
NR_120592.1:n.630-397G>C (PRSS23)
NR_120591.2:n.578+320G>C (PRSS23)
NR_120592.2:n.328-397G>C (PRSS23)
NM_012193.4:c.*323C>G (FZD4) MANE Select NP_036325.2:n.*323C>G
NR_120591.3:n.578+320G>C (PRSS23)