Canonical Allele Identifier: CA1988808946

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86952139T= , CM000673.2:g.86952139T= GRCh38
NC_000011.9:g.86663181T= , CM000673.1:g.86663181T= GRCh37
NC_000011.8:g.86340829T= NCBI36
NG_011752.1:g.8253A=

Transcript Alleles

HGVS Amino-acid change
ENST00000531380.2:c.617A= (FZD4) MANE Select ENSP00000434034.1:p.Tyr206=
ENST00000531380.1:c.617A= (FZD4) ENSP00000434034.1:p.Tyr206=
ENST00000532234.5:c.*1132T= (PRSS23) ENSP00000436676.1:n.*1132T=
ENST00000533902.2:c.*854T= (PRSS23) ENSP00000437268.1:n.*854T=
NM_012193.3:c.617A= (FZD4) NP_036325.2:p.Tyr206=
NR_120591.1:n.1804T= (PRSS23)
NR_120592.1:n.1553T= (PRSS23)
NR_120591.2:n.1502T= (PRSS23)
NR_120592.2:n.1251T= (PRSS23)
NM_012193.4:c.617A= (FZD4) MANE Select NP_036325.2:p.Tyr206=
NR_120591.3:n.1502T= (PRSS23)