Canonical Allele Identifier: CA382011784

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951440A>C , CM000673.2:g.86951440A>C GRCh38
NC_000011.9:g.86662482A>C , CM000673.1:g.86662482A>C GRCh37
NC_000011.8:g.86340130A>C NCBI36
NG_011752.1:g.8952T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.1316T>G (FZD4) MANE Select ENSP00000434034.1:p.Val439Gly
ENST00000531380.1:c.1316T>G (FZD4) ENSP00000434034.1:p.Val439Gly
ENST00000531521.1:n.611A>C (PRSS23)
ENST00000532234.5:c.*433A>C (PRSS23) ENSP00000436676.1:n.*433A>C
ENST00000533902.2:c.*155A>C (PRSS23) ENSP00000437268.1:n.*155A>C
NM_012193.3:c.1316T>G (FZD4) NP_036325.2:p.Val439Gly
NR_120591.1:n.1105A>C (PRSS23)
NR_120592.1:n.854A>C (PRSS23)
NR_120591.2:n.803A>C (PRSS23)
NR_120592.2:n.552A>C (PRSS23)
NM_012193.4:c.1316T>G (FZD4) MANE Select NP_036325.2:p.Val439Gly
NR_120591.3:n.803A>C (PRSS23)