Canonical Allele Identifier: CA382017502

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86952460C>G , CM000673.2:g.86952460C>G GRCh38
NC_000011.9:g.86663502C>G , CM000673.1:g.86663502C>G GRCh37
NC_000011.8:g.86341150C>G NCBI36
NG_011752.1:g.7932G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000531380.2:c.296G>C (FZD4) MANE Select ENSP00000434034.1:p.Cys99Ser
ENST00000531380.1:c.296G>C (FZD4) ENSP00000434034.1:p.Cys99Ser
ENST00000532234.5:c.*1453C>G (PRSS23) ENSP00000436676.1:n.*1453C>G
ENST00000533902.2:c.*1175C>G (PRSS23) ENSP00000437268.1:n.*1175C>G
NM_012193.3:c.296G>C (FZD4) NP_036325.2:p.Cys99Ser
NR_120591.1:n.2125C>G (PRSS23)
NR_120592.1:n.1874C>G (PRSS23)
NR_120591.2:n.1823C>G (PRSS23)
NR_120592.2:n.1572C>G (PRSS23)
NM_012193.4:c.296G>C (FZD4) MANE Select NP_036325.2:p.Cys99Ser
NR_120591.3:n.1823C>G (PRSS23)