Canonical Allele Identifier: CA1988807817

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951329A= , CM000673.2:g.86951329A= GRCh38
NC_000011.9:g.86662371A= , CM000673.1:g.86662371A= GRCh37
NC_000011.8:g.86340019A= NCBI36
NG_011752.1:g.9063T=

Transcript Alleles

HGVS Amino-acid change
ENST00000531380.2:c.1427T= (FZD4) MANE Select ENSP00000434034.1:p.Val476=
ENST00000528769.5:n.386A= (PRSS23)
ENST00000531380.1:c.1427T= (FZD4) ENSP00000434034.1:p.Val476=
ENST00000531521.1:n.500A= (PRSS23)
ENST00000532234.5:c.*322A= (PRSS23) ENSP00000436676.1:n.*322A=
ENST00000533902.2:c.*44A= (PRSS23) ENSP00000437268.1:n.*44A=
NM_012193.3:c.1427T= (FZD4) NP_036325.2:p.Val476=
NR_120591.1:n.994A= (PRSS23)
NR_120592.1:n.743A= (PRSS23)
NR_120591.2:n.692A= (PRSS23)
NR_120592.2:n.441A= (PRSS23)
NM_012193.4:c.1427T= (FZD4) MANE Select NP_036325.2:p.Val476=
NR_120591.3:n.692A= (PRSS23)