Canonical Allele Identifier: CA1988807756

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951279T= , CM000673.2:g.86951279T= GRCh38
NC_000011.9:g.86662321T= , CM000673.1:g.86662321T= GRCh37
NC_000011.8:g.86339969T= NCBI36
NG_011752.1:g.9113A=

Transcript Alleles

HGVS Amino-acid change
ENST00000531380.2:c.1477A= (FZD4) MANE Select ENSP00000434034.1:p.Met493=
ENST00000528769.5:n.336T= (PRSS23)
ENST00000531380.1:c.1477A= (FZD4) ENSP00000434034.1:p.Met493=
ENST00000531521.1:n.450T= (PRSS23)
ENST00000532234.5:c.*272T= (PRSS23) ENSP00000436676.1:n.*272T=
ENST00000533902.2:c.270T= (PRSS23) ENSP00000437268.1:p.His90=
NM_012193.3:c.1477A= (FZD4) NP_036325.2:p.Met493=
NR_120591.1:n.944T= (PRSS23)
NR_120592.1:n.693T= (PRSS23)
NR_120591.2:n.642T= (PRSS23)
NR_120592.2:n.391T= (PRSS23)
NM_012193.4:c.1477A= (FZD4) MANE Select NP_036325.2:p.Met493=
NR_120591.3:n.642T= (PRSS23)