Canonical Allele Identifier: CA382015705

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86952217T>A , CM000673.2:g.86952217T>A GRCh38
NC_000011.9:g.86663259T>A , CM000673.1:g.86663259T>A GRCh37
NC_000011.8:g.86340907T>A NCBI36
NG_011752.1:g.8175A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000531380.2:c.539A>T (FZD4) MANE Select ENSP00000434034.1:p.Glu180Val
ENST00000531380.1:c.539A>T (FZD4) ENSP00000434034.1:p.Glu180Val
ENST00000532234.5:c.*1210T>A (PRSS23) ENSP00000436676.1:n.*1210T>A
ENST00000533902.2:c.*932T>A (PRSS23) ENSP00000437268.1:n.*932T>A
NM_012193.3:c.539A>T (FZD4) NP_036325.2:p.Glu180Val
NR_120591.1:n.1882T>A (PRSS23)
NR_120592.1:n.1631T>A (PRSS23)
NR_120591.2:n.1580T>A (PRSS23)
NR_120592.2:n.1329T>A (PRSS23)
NM_012193.4:c.539A>T (FZD4) MANE Select NP_036325.2:p.Glu180Val
NR_120591.3:n.1580T>A (PRSS23)