Canonical Allele Identifier: CA2615461575

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951563_86951570del , CM000673.2:g.86951563_86951570del GRCh38
NC_000011.9:g.86662605_86662612del , CM000673.1:g.86662605_86662612del GRCh37
NC_000011.8:g.86340253_86340260del NCBI36
NG_011752.1:g.8825_8832del

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.1189_1196del (FZD4) MANE Select ENSP00000434034.1:p.Thr397GlyfsTer?
ENST00000531380.1:c.1189_1196del (FZD4) ENSP00000434034.1:p.Thr397GlyfsTer?
ENST00000531521.1:n.734_741del (PRSS23)
ENST00000532234.5:c.*556_*563del (PRSS23) ENSP00000436676.1:n.*556_*563del
ENST00000533902.2:c.*278_*285del (PRSS23) ENSP00000437268.1:n.*278_*285del
NM_012193.3:c.1189_1196del (FZD4) NP_036325.2:p.Thr397GlyfsTer?
NR_120591.1:n.1228_1235del (PRSS23)
NR_120592.1:n.977_984del (PRSS23)
NR_120591.2:n.926_933del (PRSS23)
NR_120592.2:n.675_682del (PRSS23)
NM_012193.4:c.1189_1196del (FZD4) MANE Select NP_036325.2:p.Thr397GlyfsTer?
NR_120591.3:n.926_933del (PRSS23)