Canonical Allele Identifier: CA382016233

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86952292T>G , CM000673.2:g.86952292T>G GRCh38
NC_000011.9:g.86663334T>G , CM000673.1:g.86663334T>G GRCh37
NC_000011.8:g.86340982T>G NCBI36
NG_011752.1:g.8100A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.464A>C (FZD4) MANE Select ENSP00000434034.1:p.Asn155Thr
ENST00000531380.1:c.464A>C (FZD4) ENSP00000434034.1:p.Asn155Thr
ENST00000532234.5:c.*1285T>G (PRSS23) ENSP00000436676.1:n.*1285T>G
ENST00000533902.2:c.*1007T>G (PRSS23) ENSP00000437268.1:n.*1007T>G
NM_012193.3:c.464A>C (FZD4) NP_036325.2:p.Asn155Thr
NR_120591.1:n.1957T>G (PRSS23)
NR_120592.1:n.1706T>G (PRSS23)
NR_120591.2:n.1655T>G (PRSS23)
NR_120592.2:n.1404T>G (PRSS23)
NM_012193.4:c.464A>C (FZD4) MANE Select NP_036325.2:p.Asn155Thr
NR_120591.3:n.1655T>G (PRSS23)