Canonical Allele Identifier: CA1988807727

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951264C= , CM000673.2:g.86951264C= GRCh38
NC_000011.9:g.86662306C= , CM000673.1:g.86662306C= GRCh37
NC_000011.8:g.86339954C= NCBI36
NG_011752.1:g.9128G=

Transcript Alleles

HGVS Amino-acid change
ENST00000531380.2:c.1492G= (FZD4) MANE Select ENSP00000434034.1:p.Ala498=
ENST00000528769.5:n.321C= (PRSS23)
ENST00000531380.1:c.1492G= (FZD4) ENSP00000434034.1:p.Ala498=
ENST00000531521.1:n.435C= (PRSS23)
ENST00000532234.5:c.*257C= (PRSS23) ENSP00000436676.1:n.*257C=
ENST00000533902.2:c.255C= (PRSS23) ENSP00000437268.1:p.Gly85=
NM_012193.3:c.1492G= (FZD4) NP_036325.2:p.Ala498=
NR_120591.1:n.929C= (PRSS23)
NR_120592.1:n.678C= (PRSS23)
NR_120591.2:n.627C= (PRSS23)
NR_120592.2:n.376C= (PRSS23)
NM_012193.4:c.1492G= (FZD4) MANE Select NP_036325.2:p.Ala498=
NR_120591.3:n.627C= (PRSS23)