Canonical Allele Identifier: CA382010976

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951230T>G , CM000673.2:g.86951230T>G GRCh38
NC_000011.9:g.86662272T>G , CM000673.1:g.86662272T>G GRCh37
NC_000011.8:g.86339920T>G NCBI36
NG_011752.1:g.9162A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000531380.2:c.1526A>C (FZD4) MANE Select ENSP00000434034.1:p.Asn509Thr
ENST00000528769.5:n.287T>G (PRSS23)
ENST00000531380.1:c.1526A>C (FZD4) ENSP00000434034.1:p.Asn509Thr
ENST00000531521.1:n.401T>G (PRSS23)
ENST00000532234.5:c.*223T>G (PRSS23) ENSP00000436676.1:n.*223T>G
ENST00000533902.2:c.221T>G (PRSS23) ENSP00000437268.1:p.Val74Gly
NM_012193.3:c.1526A>C (FZD4) NP_036325.2:p.Asn509Thr
NR_120591.1:n.895T>G (PRSS23)
NR_120592.1:n.644T>G (PRSS23)
NR_120591.2:n.593T>G (PRSS23)
NR_120592.2:n.342T>G (PRSS23)
NM_012193.4:c.1526A>C (FZD4) MANE Select NP_036325.2:p.Asn509Thr
NR_120591.3:n.593T>G (PRSS23)