Canonical Allele Identifier: CA1988807828

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951335A= , CM000673.2:g.86951335A= GRCh38
NC_000011.9:g.86662377A= , CM000673.1:g.86662377A= GRCh37
NC_000011.8:g.86340025A= NCBI36
NG_011752.1:g.9057T=

Transcript Alleles

HGVS Amino-acid change
ENST00000531380.2:c.1421T= (FZD4) MANE Select ENSP00000434034.1:p.Met474=
ENST00000528769.5:n.392A= (PRSS23)
ENST00000531380.1:c.1421T= (FZD4) ENSP00000434034.1:p.Met474=
ENST00000531521.1:n.506A= (PRSS23)
ENST00000532234.5:c.*328A= (PRSS23) ENSP00000436676.1:n.*328A=
ENST00000533902.2:c.*50A= (PRSS23) ENSP00000437268.1:n.*50A=
NM_012193.3:c.1421T= (FZD4) NP_036325.2:p.Met474=
NR_120591.1:n.1000A= (PRSS23)
NR_120592.1:n.749A= (PRSS23)
NR_120591.2:n.698A= (PRSS23)
NR_120592.2:n.447A= (PRSS23)
NM_012193.4:c.1421T= (FZD4) MANE Select NP_036325.2:p.Met474=
NR_120591.3:n.698A= (PRSS23)