Canonical Allele Identifier: CA382012598

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951570A>C , CM000673.2:g.86951570A>C GRCh38
NC_000011.9:g.86662612A>C , CM000673.1:g.86662612A>C GRCh37
NC_000011.8:g.86340260A>C NCBI36
NG_011752.1:g.8822T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.1186T>G (FZD4) MANE Select ENSP00000434034.1:p.Phe396Val
ENST00000531380.1:c.1186T>G (FZD4) ENSP00000434034.1:p.Phe396Val
ENST00000531521.1:n.741A>C (PRSS23)
ENST00000532234.5:c.*563A>C (PRSS23) ENSP00000436676.1:n.*563A>C
ENST00000533902.2:c.*285A>C (PRSS23) ENSP00000437268.1:n.*285A>C
NM_012193.3:c.1186T>G (FZD4) NP_036325.2:p.Phe396Val
NR_120591.1:n.1235A>C (PRSS23)
NR_120592.1:n.984A>C (PRSS23)
NR_120591.2:n.933A>C (PRSS23)
NR_120592.2:n.682A>C (PRSS23)
NM_012193.4:c.1186T>G (FZD4) MANE Select NP_036325.2:p.Phe396Val
NR_120591.3:n.933A>C (PRSS23)