Canonical Allele Identifier: CA382011702

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951426A>G , CM000673.2:g.86951426A>G GRCh38
NC_000011.9:g.86662468A>G , CM000673.1:g.86662468A>G GRCh37
NC_000011.8:g.86340116A>G NCBI36
NG_011752.1:g.8966T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.1330T>C (FZD4) MANE Select ENSP00000434034.1:p.Tyr444His
ENST00000531380.1:c.1330T>C (FZD4) ENSP00000434034.1:p.Tyr444His
ENST00000531521.1:n.597A>G (PRSS23)
ENST00000532234.5:c.*419A>G (PRSS23) ENSP00000436676.1:n.*419A>G
ENST00000533902.2:c.*141A>G (PRSS23) ENSP00000437268.1:n.*141A>G
NM_012193.3:c.1330T>C (FZD4) NP_036325.2:p.Tyr444His
NR_120591.1:n.1091A>G (PRSS23)
NR_120592.1:n.840A>G (PRSS23)
NR_120591.2:n.789A>G (PRSS23)
NR_120592.2:n.538A>G (PRSS23)
NM_012193.4:c.1330T>C (FZD4) MANE Select NP_036325.2:p.Tyr444His
NR_120591.3:n.789A>G (PRSS23)