Canonical Allele Identifier: CA382010979

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951231T>C , CM000673.2:g.86951231T>C GRCh38
NC_000011.9:g.86662273T>C , CM000673.1:g.86662273T>C GRCh37
NC_000011.8:g.86339921T>C NCBI36
NG_011752.1:g.9161A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000531380.2:c.1525A>G (FZD4) MANE Select ENSP00000434034.1:p.Asn509Asp
ENST00000528769.5:n.288T>C (PRSS23)
ENST00000531380.1:c.1525A>G (FZD4) ENSP00000434034.1:p.Asn509Asp
ENST00000531521.1:n.402T>C (PRSS23)
ENST00000532234.5:c.*224T>C (PRSS23) ENSP00000436676.1:n.*224T>C
ENST00000533902.2:c.222T>C (PRSS23) ENSP00000437268.1:p.Val74=
NM_012193.3:c.1525A>G (FZD4) NP_036325.2:p.Asn509Asp
NR_120591.1:n.896T>C (PRSS23)
NR_120592.1:n.645T>C (PRSS23)
NR_120591.2:n.594T>C (PRSS23)
NR_120592.2:n.343T>C (PRSS23)
NM_012193.4:c.1525A>G (FZD4) MANE Select NP_036325.2:p.Asn509Asp
NR_120591.3:n.594T>C (PRSS23)