Canonical Allele Identifier: CA382015771

Linked Data

ClinVar Variation Id: 2009890
ClinVar RCV Id: RCV002842758

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86952226G>C , CM000673.2:g.86952226G>C GRCh38
NC_000011.9:g.86663268G>C , CM000673.1:g.86663268G>C GRCh37
NC_000011.8:g.86340916G>C NCBI36
NG_011752.1:g.8166C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000531380.2:c.530C>G (FZD4) MANE Select ENSP00000434034.1:p.Pro177Arg
ENST00000531380.1:c.530C>G (FZD4) ENSP00000434034.1:p.Pro177Arg
ENST00000532234.5:c.*1219G>C (PRSS23) ENSP00000436676.1:n.*1219G>C
ENST00000533902.2:c.*941G>C (PRSS23) ENSP00000437268.1:n.*941G>C
NM_012193.3:c.530C>G (FZD4) NP_036325.2:p.Pro177Arg
NR_120591.1:n.1891G>C (PRSS23)
NR_120592.1:n.1640G>C (PRSS23)
NR_120591.2:n.1589G>C (PRSS23)
NR_120592.2:n.1338G>C (PRSS23)
NM_012193.4:c.530C>G (FZD4) MANE Select NP_036325.2:p.Pro177Arg
NR_120591.3:n.1589G>C (PRSS23)