Canonical Allele Identifier: CA1988809099

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86952233T= , CM000673.2:g.86952233T= GRCh38
NC_000011.9:g.86663275T= , CM000673.1:g.86663275T= GRCh37
NC_000011.8:g.86340923T= NCBI36
NG_011752.1:g.8159A=

Transcript Alleles

HGVS Amino-acid change
ENST00000531380.2:c.523A= (FZD4) MANE Select ENSP00000434034.1:p.Ile175=
ENST00000531380.1:c.523A= (FZD4) ENSP00000434034.1:p.Ile175=
ENST00000532234.5:c.*1226T= (PRSS23) ENSP00000436676.1:n.*1226T=
ENST00000533902.2:c.*948T= (PRSS23) ENSP00000437268.1:n.*948T=
NM_012193.3:c.523A= (FZD4) NP_036325.2:p.Ile175=
NR_120591.1:n.1898T= (PRSS23)
NR_120592.1:n.1647T= (PRSS23)
NR_120591.2:n.1596T= (PRSS23)
NR_120592.2:n.1345T= (PRSS23)
NM_012193.4:c.523A= (FZD4) MANE Select NP_036325.2:p.Ile175=
NR_120591.3:n.1596T= (PRSS23)