Canonical Allele Identifier: CA382011274

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951325T>A , CM000673.2:g.86951325T>A GRCh38
NC_000011.9:g.86662367T>A , CM000673.1:g.86662367T>A GRCh37
NC_000011.8:g.86340015T>A NCBI36
NG_011752.1:g.9067A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000531380.2:c.1431A>T (FZD4) MANE Select ENSP00000434034.1:p.Glu477Asp
ENST00000528769.5:n.382T>A (PRSS23)
ENST00000531380.1:c.1431A>T (FZD4) ENSP00000434034.1:p.Glu477Asp
ENST00000531521.1:n.496T>A (PRSS23)
ENST00000532234.5:c.*318T>A (PRSS23) ENSP00000436676.1:n.*318T>A
ENST00000533902.2:c.*40T>A (PRSS23) ENSP00000437268.1:n.*40T>A
NM_012193.3:c.1431A>T (FZD4) NP_036325.2:p.Glu477Asp
NR_120591.1:n.990T>A (PRSS23)
NR_120592.1:n.739T>A (PRSS23)
NR_120591.2:n.688T>A (PRSS23)
NR_120592.2:n.437T>A (PRSS23)
NM_012193.4:c.1431A>T (FZD4) MANE Select NP_036325.2:p.Glu477Asp
NR_120591.3:n.688T>A (PRSS23)