Canonical Allele Identifier: CA382011522

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.1364A>C (FZD4) MANE Select ENSP00000434034.1:p.Tyr455Ser
ENST00000528769.5:n.449T>G (PRSS23)
ENST00000531380.1:c.1364A>C (FZD4) ENSP00000434034.1:p.Tyr455Ser
ENST00000531521.1:n.563T>G (PRSS23)
ENST00000532234.5:c.*385T>G (PRSS23) ENSP00000436676.1:n.*385T>G
ENST00000533902.2:c.*107T>G (PRSS23) ENSP00000437268.1:n.*107T>G
NM_012193.3:c.1364A>C (FZD4) NP_036325.2:p.Tyr455Ser
NR_120591.1:n.1057T>G (PRSS23)
NR_120592.1:n.806T>G (PRSS23)
NR_120591.2:n.755T>G (PRSS23)
NR_120592.2:n.504T>G (PRSS23)
NM_012193.4:c.1364A>C (FZD4) MANE Select NP_036325.2:p.Tyr455Ser
NR_120591.3:n.755T>G (PRSS23)