Canonical Allele Identifier: CA1988807779

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951291T= , CM000673.2:g.86951291T= GRCh38
NC_000011.9:g.86662333T= , CM000673.1:g.86662333T= GRCh37
NC_000011.8:g.86339981T= NCBI36
NG_011752.1:g.9101A=

Transcript Alleles

HGVS Amino-acid change
ENST00000531380.2:c.1465A= (FZD4) MANE Select ENSP00000434034.1:p.Ile489=
ENST00000528769.5:n.348T= (PRSS23)
ENST00000531380.1:c.1465A= (FZD4) ENSP00000434034.1:p.Ile489=
ENST00000531521.1:n.462T= (PRSS23)
ENST00000532234.5:c.*284T= (PRSS23) ENSP00000436676.1:n.*284T=
ENST00000533902.2:c.*6T= (PRSS23) ENSP00000437268.1:n.*6T=
NM_012193.3:c.1465A= (FZD4) NP_036325.2:p.Ile489=
NR_120591.1:n.956T= (PRSS23)
NR_120592.1:n.705T= (PRSS23)
NR_120591.2:n.654T= (PRSS23)
NR_120592.2:n.403T= (PRSS23)
NM_012193.4:c.1465A= (FZD4) MANE Select NP_036325.2:p.Ile489=
NR_120591.3:n.654T= (PRSS23)