Canonical Allele Identifier: CA1988808068

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951492T= , CM000673.2:g.86951492T= GRCh38
NC_000011.9:g.86662534T= , CM000673.1:g.86662534T= GRCh37
NC_000011.8:g.86340182T= NCBI36
NG_011752.1:g.8900A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.1264A= (FZD4) MANE Select ENSP00000434034.1:p.Lys422=
ENST00000531380.1:c.1264A= (FZD4) ENSP00000434034.1:p.Lys422=
ENST00000531521.1:n.663T= (PRSS23)
ENST00000532234.5:c.*485T= (PRSS23) ENSP00000436676.1:n.*485T=
ENST00000533902.2:c.*207T= (PRSS23) ENSP00000437268.1:n.*207T=
NM_012193.3:c.1264A= (FZD4) NP_036325.2:p.Lys422=
NR_120591.1:n.1157T= (PRSS23)
NR_120592.1:n.906T= (PRSS23)
NR_120591.2:n.855T= (PRSS23)
NR_120592.2:n.604T= (PRSS23)
NM_012193.4:c.1264A= (FZD4) MANE Select NP_036325.2:p.Lys422=
NR_120591.3:n.855T= (PRSS23)