Canonical Allele Identifier: CA1988808074

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951496A= , CM000673.2:g.86951496A= GRCh38
NC_000011.9:g.86662538A= , CM000673.1:g.86662538A= GRCh37
NC_000011.8:g.86340186A= NCBI36
NG_011752.1:g.8896T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.1260T= (FZD4) MANE Select ENSP00000434034.1:p.Leu420=
ENST00000531380.1:c.1260T= (FZD4) ENSP00000434034.1:p.Leu420=
ENST00000531521.1:n.667A= (PRSS23)
ENST00000532234.5:c.*489A= (PRSS23) ENSP00000436676.1:n.*489A=
ENST00000533902.2:c.*211A= (PRSS23) ENSP00000437268.1:n.*211A=
NM_012193.3:c.1260T= (FZD4) NP_036325.2:p.Leu420=
NR_120591.1:n.1161A= (PRSS23)
NR_120592.1:n.910A= (PRSS23)
NR_120591.2:n.859A= (PRSS23)
NR_120592.2:n.608A= (PRSS23)
NM_012193.4:c.1260T= (FZD4) MANE Select NP_036325.2:p.Leu420=
NR_120591.3:n.859A= (PRSS23)