Canonical Allele Identifier: CA382014275

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951963A>G , CM000673.2:g.86951963A>G GRCh38
NC_000011.9:g.86663005A>G , CM000673.1:g.86663005A>G GRCh37
NC_000011.8:g.86340653A>G NCBI36
NG_011752.1:g.8429T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.793T>C (FZD4) MANE Select ENSP00000434034.1:p.Tyr265His
ENST00000531380.1:c.793T>C (FZD4) ENSP00000434034.1:p.Tyr265His
ENST00000532234.5:c.*956A>G (PRSS23) ENSP00000436676.1:n.*956A>G
ENST00000533902.2:c.*678A>G (PRSS23) ENSP00000437268.1:n.*678A>G
NM_012193.3:c.793T>C (FZD4) NP_036325.2:p.Tyr265His
NR_120591.1:n.1628A>G (PRSS23)
NR_120592.1:n.1377A>G (PRSS23)
NR_120591.2:n.1326A>G (PRSS23)
NR_120592.2:n.1075A>G (PRSS23)
NM_012193.4:c.793T>C (FZD4) MANE Select NP_036325.2:p.Tyr265His
NR_120591.3:n.1326A>G (PRSS23)