Canonical Allele Identifier: CA382010909

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951202C>G , CM000673.2:g.86951202C>G GRCh38
NC_000011.9:g.86662244C>G , CM000673.1:g.86662244C>G GRCh37
NC_000011.8:g.86339892C>G NCBI36
NG_011752.1:g.9190G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.1554G>C (FZD4) MANE Select ENSP00000434034.1:p.Lys518Asn
ENST00000528769.5:n.273-14C>G (PRSS23)
ENST00000531380.1:c.1554G>C (FZD4) ENSP00000434034.1:p.Lys518Asn
ENST00000531521.1:n.387-14C>G (PRSS23)
ENST00000532234.5:c.*209-14C>G (PRSS23) ENSP00000436676.1:n.*209-14C>G
ENST00000533902.2:c.207-14C>G (PRSS23) ENSP00000437268.1:n.207-14C>G
NM_012193.3:c.1554G>C (FZD4) NP_036325.2:p.Lys518Asn
NR_120591.1:n.881-14C>G (PRSS23)
NR_120592.1:n.630-14C>G (PRSS23)
NR_120591.2:n.579-14C>G (PRSS23)
NR_120592.2:n.328-14C>G (PRSS23)
NM_012193.4:c.1554G>C (FZD4) MANE Select NP_036325.2:p.Lys518Asn
NR_120591.3:n.579-14C>G (PRSS23)