Canonical Allele Identifier: CA382011321

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951338T>G , CM000673.2:g.86951338T>G GRCh38
NC_000011.9:g.86662380T>G , CM000673.1:g.86662380T>G GRCh37
NC_000011.8:g.86340028T>G NCBI36
NG_011752.1:g.9054A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.1418A>C (FZD4) MANE Select ENSP00000434034.1:p.Asn473Thr
ENST00000528769.5:n.395T>G (PRSS23)
ENST00000531380.1:c.1418A>C (FZD4) ENSP00000434034.1:p.Asn473Thr
ENST00000531521.1:n.509T>G (PRSS23)
ENST00000532234.5:c.*331T>G (PRSS23) ENSP00000436676.1:n.*331T>G
ENST00000533902.2:c.*53T>G (PRSS23) ENSP00000437268.1:n.*53T>G
NM_012193.3:c.1418A>C (FZD4) NP_036325.2:p.Asn473Thr
NR_120591.1:n.1003T>G (PRSS23)
NR_120592.1:n.752T>G (PRSS23)
NR_120591.2:n.701T>G (PRSS23)
NR_120592.2:n.450T>G (PRSS23)
NM_012193.4:c.1418A>C (FZD4) MANE Select NP_036325.2:p.Asn473Thr
NR_120591.3:n.701T>G (PRSS23)