Canonical Allele Identifier: CA1988807814

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951323A= , CM000673.2:g.86951323A= GRCh38
NC_000011.9:g.86662365A= , CM000673.1:g.86662365A= GRCh37
NC_000011.8:g.86340013A= NCBI36
NG_011752.1:g.9069T=

Transcript Alleles

HGVS Amino-acid change
ENST00000531380.2:c.1433T= (FZD4) MANE Select ENSP00000434034.1:p.Met478=
ENST00000528769.5:n.380A= (PRSS23)
ENST00000531380.1:c.1433T= (FZD4) ENSP00000434034.1:p.Met478=
ENST00000531521.1:n.494A= (PRSS23)
ENST00000532234.5:c.*316A= (PRSS23) ENSP00000436676.1:n.*316A=
ENST00000533902.2:c.*38A= (PRSS23) ENSP00000437268.1:n.*38A=
NM_012193.3:c.1433T= (FZD4) NP_036325.2:p.Met478=
NR_120591.1:n.988A= (PRSS23)
NR_120592.1:n.737A= (PRSS23)
NR_120591.2:n.686A= (PRSS23)
NR_120592.2:n.435A= (PRSS23)
NM_012193.4:c.1433T= (FZD4) MANE Select NP_036325.2:p.Met478=
NR_120591.3:n.686A= (PRSS23)