Canonical Allele Identifier: CA1988808216

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951602T= , CM000673.2:g.86951602T= GRCh38
NC_000011.9:g.86662644T= , CM000673.1:g.86662644T= GRCh37
NC_000011.8:g.86340292T= NCBI36
NG_011752.1:g.8790A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.1154A= (FZD4) MANE Select ENSP00000434034.1:p.Asp385=
ENST00000531380.1:c.1154A= (FZD4) ENSP00000434034.1:p.Asp385=
ENST00000531521.1:n.773T= (PRSS23)
ENST00000532234.5:c.*595T= (PRSS23) ENSP00000436676.1:n.*595T=
ENST00000533902.2:c.*317T= (PRSS23) ENSP00000437268.1:n.*317T=
NM_012193.3:c.1154A= (FZD4) NP_036325.2:p.Asp385=
NR_120591.1:n.1267T= (PRSS23)
NR_120592.1:n.1016T= (PRSS23)
NR_120591.2:n.965T= (PRSS23)
NR_120592.2:n.714T= (PRSS23)
NM_012193.4:c.1154A= (FZD4) MANE Select NP_036325.2:p.Asp385=
NR_120591.3:n.965T= (PRSS23)