Canonical Allele Identifier: CA1988802571

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86946480_86946483delinsGCTA , CM000673.2:g.86946480_86946483delinsGCTA GRCh38
NC_000011.9:g.86657522_86657525delinsGCTA , CM000673.1:g.86657522_86657525delinsGCTA GRCh37
NC_000011.8:g.86335170_86335173delinsGCTA NCBI36
NG_011752.1:g.13909_13912delinsTAGC

Transcript Alleles

HGVS Amino-acid change
ENST00000531380.2:c.*4659_*4662delinsTAGC (FZD4) MANE Select ENSP00000434034.1:n.*4659_*4662delinsTAGC...
ENST00000528769.5:n.129-3876_129-3873delinsGCTA (PRSS23)
ENST00000531380.1:c.*4659_*4662delinsTAGC (FZD4) ENSP00000434034.1:n.*4659_*4662delinsTAGC...
ENST00000531521.1:n.243-3876_243-3873delinsGCTA (PRSS23)
ENST00000532234.5:c.*65-3876_*65-3873delinsGCTA (PRSS23) ENSP00000436676.1:n.*65-3876_*65-3873deli...
ENST00000533902.2:c.207-4736_207-4733delinsGCTA (PRSS23) ENSP00000437268.1:n.207-4736_207-4733deli...
NM_012193.3:c.*4659_*4662delinsTAGC (FZD4) NP_036325.2:n.*4659_*4662delinsTAGC
NR_120591.1:n.737-3876_737-3873delinsGCTA (PRSS23)
NR_120592.1:n.630-4736_630-4733delinsGCTA (PRSS23)
NR_120591.2:n.435-3876_435-3873delinsGCTA (PRSS23)
NR_120592.2:n.328-4736_328-4733delinsGCTA (PRSS23)
NM_012193.4:c.*4659_*4662delinsTAGC (FZD4) MANE Select NP_036325.2:n.*4659_*4662delinsTAGC
NR_120591.3:n.435-3876_435-3873delinsGCTA (PRSS23)