Canonical Allele Identifier: CA2695215108

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951601del , CM000673.2:g.86951601del GRCh38
NC_000011.9:g.86662643del , CM000673.1:g.86662643del GRCh37
NC_000011.8:g.86340291del NCBI36
NG_011752.1:g.8791del

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.1155del (FZD4) MANE Select ENSP00000434034.1:p.Asp385GlufsTer?
ENST00000531380.1:c.1155del (FZD4) ENSP00000434034.1:p.Asp385GlufsTer?
ENST00000531521.1:n.772del (PRSS23)
ENST00000532234.5:c.*594del (PRSS23) ENSP00000436676.1:n.*594del
ENST00000533902.2:c.*316del (PRSS23) ENSP00000437268.1:n.*316del
NM_012193.3:c.1155del (FZD4) NP_036325.2:p.Asp385GlufsTer?
NR_120591.1:n.1266del (PRSS23)
NR_120592.1:n.1015del (PRSS23)
NR_120591.2:n.964del (PRSS23)
NR_120592.2:n.713del (PRSS23)
NM_012193.4:c.1155del (FZD4) MANE Select NP_036325.2:p.Asp385GlufsTer?
NR_120591.3:n.964del (PRSS23)