Canonical Allele Identifier: CA1988808224

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951603C= , CM000673.2:g.86951603C= GRCh38
NC_000011.9:g.86662645C= , CM000673.1:g.86662645C= GRCh37
NC_000011.8:g.86340293C= NCBI36
NG_011752.1:g.8789G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.1153G= (FZD4) MANE Select ENSP00000434034.1:p.Asp385=
ENST00000531380.1:c.1153G= (FZD4) ENSP00000434034.1:p.Asp385=
ENST00000531521.1:n.774C= (PRSS23)
ENST00000532234.5:c.*596C= (PRSS23) ENSP00000436676.1:n.*596C=
ENST00000533902.2:c.*318C= (PRSS23) ENSP00000437268.1:n.*318C=
NM_012193.3:c.1153G= (FZD4) NP_036325.2:p.Asp385=
NR_120591.1:n.1268C= (PRSS23)
NR_120592.1:n.1017C= (PRSS23)
NR_120591.2:n.966C= (PRSS23)
NR_120592.2:n.715C= (PRSS23)
NM_012193.4:c.1153G= (FZD4) MANE Select NP_036325.2:p.Asp385=
NR_120591.3:n.966C= (PRSS23)